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EAOJ; Vol. 6: March 2012 39 East African Orthopaedic Journal SPRENGELS SHOULDER AT THE KENYATTA NATIONAL HOSPITAL; A CASE REPORT H. O. Ong’ang’o, MMed(Surg), MSc Ortho(London), FCS-ECSA, Consultant Orthopaedic and Trauma Surgeon, Orthopaedics Department, Kenyatta National Hospital, and Honorary Lecturer in Orthopaedics, Department of Orthopaedics, University of Nairobi and Orthopaedics Department, Kenyatta National Hospital, P. O. Box 20723 - 00202, Nairobi, Kenya Correspondence to: Dr. H. O. Ong’ang’o, P. O. Box 74037-00200 Nairobi ,Kenya E-mail: herbertongango@yahoo. com. ABSTRACT Sprengel’s deformity is a rare complex congenital deformity of the shoulder girdle. It raises cosmetic conerns and occassions functional disability. Management is challenging at whatever age treatment is sought. Experience of surgeons is limited to one technical procedure and few cases of short-term follow-up. This study presents a male patient who presented at the Kenyatta National Hospital at the age of seventeen years and was managed by the Woodward’s procedure INTRODUCTION Congenital elevation of the scapula is a complex congenital deformity of the shoulder girdle. Other names attributed to it include undescended scapula, elevated scapula, Congenital high scapula and congenital undescended scapula (1-19 ). Since 1891, sprengels deformity has become like a universal eponym for this condition . In this condition, the scapula,which arises as a cervical appendage, fails to migrate caudally to its normal position on the thorax during early development. Despite its rarity, it is considered the most frequently encountered congenital deformity of the shoulder girdle( 4,8,17). The scapula is abnormally and permanently elevated(2), bilaterally in some instances. It is in addition small with a smaller vertical diameter and an apparently greater width. It is also usually adducted to some degree ( 3), with the lower pole medially rotated, causing the glenoid to face inferiorly (4). An omovertebral bone may be present joining the vertebral border of the scapula to one of the cervical vertebrae (4 ,8 ,15,17 ). Elevation of the scapula almost always occurs sporadically, though combination with other congenital anomalies,such as failure of fusion in the midline of the laminae of some cervical vertebrae, cranium bifidum, and defects in the upper dorsal vertebrae; and with developmental anomalies of the thoracic outlet, such as cervical ribs and abnormal first thoracic ribs, hemivertebrae, congenital scoliosis,fusion of ribs and irregular vertebral segmentation is usual(1,4,8,9,15). Also conditions like Klippel-Feil syndrome, kidney abnormalities, anal stenosis and cleft palate may coexist (4,6,15). It has been noted that these abnormalities may be more significant to the child’s general health than the obvious scapula deformity (18). Developmental defects of the Shoulder musculature may exist. These may affect the trapezius,the rhomboids, the levator scapulae majorly, and the serratus anterior, pectoralis major, pectoralis minor, latissimus dorsi and the sternocleidomastoid to a minor extent (5,6,9 ,15 ). The upward elevation of the scapula produces an assymetry of the shoulder which is evident at birth and progresses with growth (2).There is also impairment of shoulder function, but it is the undesirable cosmetic appearance that forces the parents to seek medical attention for their child (1). More females are affected than males with a 3:1 ratio (4,6,9). At a later age, even if there is no functional impairment, the appearance of this deformity may be sufficiently objectionable to create psychological problems (3). Radiological evaluation of these patients mainly entails plain X-rays, though a scarcity details especially of the omovertebral bone are obtained on 3D CT scan(4, 5, 10). MRI adds value when the omovertebral connection is cartilaginous or is just a fibrous band (5). Despite having been first described in 1863 (2,5,8 ,15 ), it is only in 1972 that Cavendish (6 ) devised a classification for the Sprengel deformity. No surgical treatment is adviced for Grade 1, while Surgery is adviced for Grades 2 and 3 (2,6). Surgery is discouraged for severe Grade 4, as they are said to be unlikely to Case Report : P. Wabomba, MMed (Surg), FRCS (Edin) Honorary Consultant Surgeon, Orthopaedics Department, Kenyatta National Hospital, P.O. Box 20723 - 00202, Nairobi, Kenya P.O. Box 74037-00200, Nairobi, Kenya.

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Page 1: 77828-180474-1-PB

EAOJ; Vol. 6: March 2012 39

East African Orthopaedic Journal

42 EAOJ; Vol. 6: March 2012

SPRENGELS SHOULDER AT THE KENYATTA NATIONAL HOSPITAL; A CASE REPORT

H. O. Ong’ang’o, MMed(Surg), MSc Ortho(London), FCS-ECSA, Consultant Orthopaedic and Trauma Surgeon, Orthopaedics Department, Kenyatta National Hospital, and Honorary Lecturer in Orthopaedics, Department of Orthopaedics, University of Nairobi and Peter Wabomba, MMed(Surg), FRCS(Edin) Honorary Consultant Surgeon, Orthopaedics Department, Kenyatta National Hospital, P. O. Box 20723 - 00202, Nairobi, Kenya

Correspondence to: Dr. H. O. Ong’ang’o, P. O. Box 74037-00200 Nairobi ,Kenya E-mail: herbertongango@yahoo. com.

ABSTRACTSprengel’s deformity is a rare complex congenital deformity of the shoulder girdle. It raises cosmetic

conerns and occassions functional disability. Management is challenging at whatever age treatment

is sought. Experience of surgeons is limited to one technical procedure and few cases of short-term

follow-up. This study presents a male patient who presented at the Kenyatta National Hospital at the

age of seventeen years and was managed by the Woodward’s procedure

INTRODUCTIONCongenital elevation of the scapula is a complex

congenital deformity of the shoulder girdle. Other

names attributed to it include undescended scapula,

elevated scapula, Congenital high scapula and

congenital undescended scapula (1-19 ). Since 1891,

sprengels deformity has become like a universal

eponym for this condition . In this condition, the

scapula,which arises as a cervical appendage, fails to

migrate caudally to its normal position on the thorax

during early development. Despite its rarity, it is

considered the most frequently encountered congenital

deformity of the shoulder girdle( 4,8,17). The scapula is

abnormally and permanently elevated(2), bilaterally

in some instances. It is in addition small with a smaller

vertical diameter and an apparently greater width. It

is also usually adducted to some degree ( 3), with the

lower pole medially rotated, causing the glenoid to face

inferiorly (4). An omovertebral bone may be present

joining the vertebral border of the scapula to one of the

cervical vertebrae (4 ,8 ,15,17 ).

Elevation of the scapula almost always occurs

sporadically, though combination with other congenital

anomalies,such as failure of fusion in the midline of the

laminae of some cervical vertebrae, cranium bifidum,

and defects in the upper dorsal vertebrae; and with

developmental anomalies of the thoracic outlet,

such as cervical ribs and abnormal first thoracic ribs,

hemivertebrae, congenital scoliosis,fusion of ribs and

irregular vertebral segmentation is usual(1,4,8,9,15).

Also conditions like Klippel-Feil syndrome, kidney

abnormalities, anal stenosis and cleft palate may coexist

(4,6,15). It has been noted that these abnormalities may

be more significant to the child’s general health than

the obvious scapula deformity (18). Developmental

defects of the Shoulder musculature may exist. These

may affect the trapezius,the rhomboids, the levator

scapulae majorly, and the serratus anterior, pectoralis

major, pectoralis minor, latissimus dorsi and the

sternocleidomastoid to a minor extent (5,6,9 ,15 ).

The upward elevation of the scapula produces

an assymetry of the shoulder which is evident at birth

and progresses with growth (2). There is also impairment

of shoulder function, but it is the undesirable cosmetic

appearance that forces the parents to seek medical

attention for their child (1). More females are affected

than males with a 3:1 ratio (4,6,9). At a later age, even if

there is no functional impairment, the appearance of this

deformity may be sufficiently objectionable to create

psychological problems (3). Radiological evaluation

of these patients mainly entails plain X-rays, though a

scarcity details especially of the omovertebral bone are

obtained on 3D CT scan(4, 5, 10). MRI adds value when

the omovertebral connection is cartilaginous or is just

a fibrous band (5).

Despite having been first described in 1863

(2,5,8 ,15 ), it is only in 1972 that Cavendish (6 ) devised

a classification for the Sprengel deformity. No surgical

treatment is adviced for Grade 1, while Surgery is

adviced for Grades 2 and 3 (2,6). Surgery is discouraged

for severe Grade 4, as they are said to be unlikely to

Case Report

:

P. Wabomba, MMed (Surg), FRCS (Edin) Honorary Consultant Surgeon, Orthopaedics Department, Kenyatta National Hospital, P.O. Box 20723 - 00202, Nairobi, Kenya

P.O. Box 74037-00200, Nairobi, Kenya.

East African Orthopaedic Journal

EAOJ; Vol. 6: March 2012 55

3. Tramadol 50 mg 8 hourly

4. Pantoprazole or esomeprazole 40 mg once daily

before food

An opioid like morphine or pethidine given

intraoperatively adds to the postoperative analgesic

effect. In the immediate post-operative period (48-72

hours) the following treatment is added:

5. Morphine 2-4 mg IV infusion every hour

6. Ondasentron 4 mg or metoclopramide 10 mg

Accelerated rehabilitation

Rehabilitation means restoration back to health. It

is therefore, therapy aimed at improving physical

and neurocognitive function that has been lost or

diminished by disease or traumatic injury. Accelerated

rehabilitation therefore, is shortening the period of

rehabilitation so that the patient can gain function and

independence as soon as possible. To achieve this goal

the patient must be well motivated and without pain.

There are prerequisite for patients to participate in

an accelerated rehabilitation program. They must be

educated on the effect and value of non-pharmacological

methods of restoration to function. Even with some

pain that most patients would consider unbearable,

the motivated patient can power through. The second

necessary factor is achieving adequate postoperative

pain control. The focus of any rehabilitation protocol

should be to control pain because this is the variable

that can be manipulated. No amount of encouragement

or education will convert unmotivated patient in pain

into a motivated one. The fact is that many patients,

especially younger, active males, could and should

participate in a rehabilitation program on the day of

surgery, provided they are medically stable. The benefits

include immediate, direct psychologic feedback to

the motivated patient, with the ultimate potential of

reducing his or her length-of stay.

CONCLUSION

Control of acute musculoskeletal pain, whether

traumatic or postoperative is more likely to be achieved

by use of modern protocols that apply existing basic

techniques. Staff education, regular assessment of

pain using formal scoring systems and multimodal

approach should result into improved quality of care.

Parenteral opioids administered by intramuscular

injection or by patient-controlled analgesia devices are

the recommended approach. Addition of perioperative

use of non-steroidal anti-inflammatory drugs enhances

pain control. Use of continuous spinal techniques is a

useful alternative in selected patients. Combinations

of techniques are the most effective with potential

benefits in terms of overall patient outcome.

REFERENCES

Conroy, J. M., Dorman, B. H., editors. Anesthesia for 1. orthopedic surgery. New York: Raven Press; 1994. p 355-65.

Topol, E. J. Failing the public health—rofecoxib, Merck, 2. and the FDA. N. Engl. J. Med. 2004; 351:1707-1709.

Evan, F., Ekman, L. and Koman, A. Acute pain following 3. musculoskeletal injuries and orthopaedic surgery. J. Bone Joint Surg. Am. 2004; 86:1316-1327.

Samad, T. A., Moore, K. A., Sapirstein, 4. et al. Interleukin-1-mediated induction of COX-2 in the CNS contributes to inflammatory pain hypersensitivity. Nature. 2001; 410: 471-475.

Cavalieri, T. A. Pain management in the elderly. 5. J. Am. Osteopath. Assoc. 2002; 102:481-485.

Skinner, H. B. and Shintani, E. Y. Results of a multimodal 6. analgesic trial involving patients with total hip or total knee arthroplasty. Am. J. Orthop. 2004; 33:85.

Sundbloom, D. M., Haikonen, S., Niemi-Pynttari, J. 7. and Tigerstedt, I. Effect of spiritual healing on chronic idiopathic pain: a medical and psychological study. Clin. J. Pain. 1994; 10: 296-302.

Bradley, J. D., Brandt, K. D., Katz, B. P., Kalasinski, L. 8. A. and Ryan, S. L. Comparison of antiinflammatory dose of ibuprofen, an analgesic dose of ibuprofen, and acetaminophen in the treatment of patients with osteoarthritis of the knee. N. Engl. J. Med. 1991; 325: 87-91.

Daly, F.F., Fountain, J.S., Murray, L., Graudins, A. and 9. Buckley, N.A. Guidelines for the management of paracetamol poisoning in Australia and New Zealand—explanation and elaboration. A consensus statement from clinical toxicologists consulting to the Australasian poisons information centres. Med. J. Aust. 2008: 188: 296–301. PMID 18312195

Chandrasekharan, N.V., Dai, H., Roos, K.L., 10. et al. COX-3, a cyclooxygenase-1 variant inhibited by acetaminophen and other analgesic/antipyretic drugs: cloning, structure, and expression. Proc. Natl. Acad. Sci. U.S.A. 2002; 99: 13926–13931.

Hubbard, R. C., Naumann, T. M., Traylor, L. and Dhadda, 11. S. Parecoxib sodium has opioid-sparing effects in patients undergoing total knee arthroplastyunder spinal anaesthesia. Br. J. Anaesth. 2003; 90:166-172.

Rasmussen, G. L., Steckner, K., Hogue, C., Torri, S. and 12.

Hubbard, R.C. Intravenous parecoxib sodium for acute

pain after orthopedic knee surgery. Am. J. Orthop. 2002;

31:336-343.

Woolf, C. J. and Chong, M. S. Preemptive analgesia-treating 13.

postoperative pain by preventing the establishment of

central sensitisation. Anesth. Analg. 1993; 77; 362-379.

Page 2: 77828-180474-1-PB

EAOJ; Vol. 6: March 201240

East African Orthopaedic Journal

EAOJ; Vol. 6: March 2012 43

derive any benefit (6). Many types of Surgical procedures

have been developed and these include Schrock (1,2),

Putti (2,6,), Smith (2), Ober(2), Inclan (2), Koenig (1,2),

McFarland (2), Chigot (2), Cabanac (2), Green(1,2,7,), Petrie

(11), Woodward (1,2,3,12,15), Modified Green(13,19),

Modified Woodward (12,18), Allan’s(6), Robinson and

associates (2), among others. The results of most of

these methods have , on the whole, been disappointing

(6). The timing of the surgery is an aspect that has also

seen no consensus, with most authors advocating the

time between three and six years (1,3, 6, 8,12,16). On

one extreme, Tachdjian (2) has proposed the surgery be

carried out at the age of six months, whereas Borges

et al (18) have advocated surgery even at seventeen

years, an age condemned by other Surgeons (13). It

is a considered point that outcome is not influenced

by the age of the patient at the time of surgery, nor

by the presence of an omovertebral bone (12). At the

other extreme, Doita et al (14) have argued that surgical

treatment of adult patients with Sprengel’s deformity

can produce good surgical results. Even then, Ross and

Cruess (9), from their largest review of surgically treated

patients, declared that it was not possible to determine

an optimum age for surgery. The same conclusion was

arrived at by Gonen et al (19).

Regardless of the technical procedure chosen nor

the time at which it is undertaken ,surgery for sprengels

shoulder is a long, challenging and demanding

undertaking requiring attention to small details (7). All

surgeons seem to firmly stick to only one procedure

(7, 8,13,18,19). Nevertheless the Green and Woodward

procedures have appeared better than the others(8,

15, 16), though Grogan et al (8) and Carson et al (15)

have declared the Woodward procedure to be the

best surgical procedure available for the correction of

congenital undescended scapula in children. Even then,

the technique chosen is varied to meet the individual

needs of the patient (7). Ahmad (17), has described a

new procedure for correcting severe Sprengel deformity.

Noted complications of surgical correction of Sprengels

deformity include unsightly keloid scars (3,9,13), Brachial

plexus palsy (12 ) and scapula winging (9). Initial results

of the surgical treatment were discouraging (3) but Ross

and Cruess noted that it was possible to significantly

improve the function of the shoulder and its position

relative to the other side ( 9).

Because of its rarity, few surgeons have gained

great experience with the condition, and published

reports have usually involved a small number of cases,

quite often all treated in like manner (7,8,9), and of

short-term followup. Only Carson et al (15), Borges et

al (18) and Gonen et al (19) have long-term follow-up

series.

It is the purpose of this study to present a case

of Sprengels deformity that presented to the Kenyatta

National Hospital at the age of seventeen years and was

managed by the Woodwards procedure.

CASE REPORTA 17 years old male patient presented to the authors in

2006, with complains of left shoulder pain and pain on

breathing. Patient had an elevated left shoulder, noticed

in childhood and at the time was experiencing limitation

in Left sholuder function. Attention for this had been

sought at the nearest Provincial General Hospital but

no intervention had been offered.

The significant past medical history was that the

patient was born with a cleft lip and palate which were

repaired in childhood.

Physical examination revealed an adolescent in

fair general condition, with an evident cleft lip repair

scar. There was a high left scapula that was fixed. There

was limited elevation of the left shoulder, with gross

atrophy of the supraspinatus and infraspinatus. There

was apparent adduction of the left scapula on posterior

inspection.The left clavicle appeared shortened and

there was fullness in the supraclavicular fossa .

Plain X-ray examination revealed a fully bony

omovertebral bone originating from the transverse

process of C6 vertebrae and tethering the medial angle

of the scapula, as well as an elevated medial portion of

the supraspinous part of the scapula.

CT scans further confirmed the presence of the

omovertebral bone. Patient was then prepared for

surgery, and later on in 2006, a Woodwards procedure

was performed on him. Immediate postoperative period

was uneventful and patient was dicharged after five

days for outpatient physiotherapy and followup.

Page 3: 77828-180474-1-PB

EAOJ; Vol. 6: March 2012 41

East African Orthopaedic Journal

44 EAOJ; Vol. 6: March 2012

Fig 1 Left sprengel shoulder. Note shortened clavicle and cleft lip repair scar.

Fig 2 Posterior view. Note supraspinous bone deformity and adduction of left scapula.

Fig 3

Note disparity in levels of lower poles of scapulae.

Fig 4X-ray. Note omovertebral bone and medial supraspinous bony deformity of scapula.

Fig 5Sprengel’s shoulder 3 years’ post operatively. No unsightly scar.

DISCUSSION

This case of Sprengel’s shoulder posed unusual

challenges. For a start it most likely is the second case

report from the African continent after the report by

Boon (4). We shared in the dilemma of Grogan et al (8)

who found it difficult to specify criteria to define the

optimal age for operative correction. Presenting at

seventeen years of age, this was well above the average

age of presentation and operation. Even though surgery

for Sprengel deformity in adults has been performed

(14), no series has short-term or long term follow-

up results to guide our approach to this case, as this

patient was very close to adulthood. Also being at an

age where the soft tissues have lost their plasticity, the

expected results of any surgical procedure would not

Figure 1

Figure 2

Figure 3

Figure 5

Figure 4

Boon et al (4). We shared in the dilemma of Grogan et al (8)

East African Orthopaedic Journal

EAOJ; Vol. 6: March 2012 43

derive any benefit (6). Many types of Surgical procedures

have been developed and these include Schrock (1,2),

Putti (2,6,), Smith (2), Ober(2), Inclan (2), Koenig (1,2),

McFarland (2), Chigot (2), Cabanac (2), Green(1,2,7,), Petrie

(11), Woodward (1,2,3,12,15), Modified Green(13,19),

Modified Woodward (12,18), Allan’s(6), Robinson and

associates (2), among others. The results of most of

these methods have , on the whole, been disappointing

(6). The timing of the surgery is an aspect that has also

seen no consensus, with most authors advocating the

time between three and six years (1,3, 6, 8,12,16). On

one extreme, Tachdjian (2) has proposed the surgery be

carried out at the age of six months, whereas Borges

et al (18) have advocated surgery even at seventeen

years, an age condemned by other Surgeons (13). It

is a considered point that outcome is not influenced

by the age of the patient at the time of surgery, nor

by the presence of an omovertebral bone (12). At the

other extreme, Doita et al (14) have argued that surgical

treatment of adult patients with Sprengel’s deformity

can produce good surgical results. Even then, Ross and

Cruess (9), from their largest review of surgically treated

patients, declared that it was not possible to determine

an optimum age for surgery. The same conclusion was

arrived at by Gonen et al (19).

Regardless of the technical procedure chosen nor

the time at which it is undertaken ,surgery for sprengels

shoulder is a long, challenging and demanding

undertaking requiring attention to small details (7). All

surgeons seem to firmly stick to only one procedure

(7, 8,13,18,19). Nevertheless the Green and Woodward

procedures have appeared better than the others(8,

15, 16), though Grogan et al (8) and Carson et al (15)

have declared the Woodward procedure to be the

best surgical procedure available for the correction of

congenital undescended scapula in children. Even then,

the technique chosen is varied to meet the individual

needs of the patient (7). Ahmad (17), has described a

new procedure for correcting severe Sprengel deformity.

Noted complications of surgical correction of Sprengels

deformity include unsightly keloid scars (3,9,13), Brachial

plexus palsy (12 ) and scapula winging (9). Initial results

of the surgical treatment were discouraging (3) but Ross

and Cruess noted that it was possible to significantly

improve the function of the shoulder and its position

relative to the other side ( 9).

Because of its rarity, few surgeons have gained

great experience with the condition, and published

reports have usually involved a small number of cases,

quite often all treated in like manner (7,8,9), and of

short-term followup. Only Carson et al (15), Borges et

al (18) and Gonen et al (19) have long-term follow-up

series.

It is the purpose of this study to present a case

of Sprengels deformity that presented to the Kenyatta

National Hospital at the age of seventeen years and was

managed by the Woodwards procedure.

CASE REPORTA 17 years old male patient presented to the authors in

2006, with complains of left shoulder pain and pain on

breathing. Patient had an elevated left shoulder, noticed

in childhood and at the time was experiencing limitation

in Left sholuder function. Attention for this had been

sought at the nearest Provincial General Hospital but

no intervention had been offered.

The significant past medical history was that the

patient was born with a cleft lip and palate which were

repaired in childhood.

Physical examination revealed an adolescent in

fair general condition, with an evident cleft lip repair

scar. There was a high left scapula that was fixed. There

was limited elevation of the left shoulder, with gross

atrophy of the supraspinatus and infraspinatus. There

was apparent adduction of the left scapula on posterior

inspection.The left clavicle appeared shortened and

there was fullness in the supraclavicular fossa .

Plain X-ray examination revealed a fully bony

omovertebral bone originating from the transverse

process of C6 vertebrae and tethering the medial angle

of the scapula, as well as an elevated medial portion of

the supraspinous part of the scapula.

CT scans further confirmed the presence of the

omovertebral bone. Patient was then prepared for

surgery, and later on in 2006, a Woodwards procedure

was performed on him. Immediate postoperative period

was uneventful and patient was dicharged after five

days for outpatient physiotherapy and followup.

Page 4: 77828-180474-1-PB

EAOJ; Vol. 6: March 201242

East African Orthopaedic Journal

EAOJ; Vol. 6: March 2012 45

be marvelous. This case displayed associated congenital

anomalies. The congenital cleft lip and palate that were

repaired in childhood have been reported as associated

before(4).The utilized modalities of investigating this

case were plain X-rays and a 3D CT scan. The information

obtained from these was deemed adequate for the

treatment planning of this case. No new information

would have been availed by conducting an MRI

examination. Muscle anomalies have been documented

as part of the sprengel deformity but no mention of

the supraspinatus and infraspinatus atrophy noted in

this case exists so far in the literature. The observed

atrophy of the supraspinatus and infraspinatus

would no doubt have a big role in determining the

postoperative outcome and gains of surgery. The choice

of the Woodwards procedure as treatment for this case

was arrived at by guidance from the literature as we

had no prior experience with Sprengel’s deformity. In

line with the practice of other surgeons, we are likely

to offer future patients the same basic procedure, with

modifications as the experience enlightens us. What

we are left wondering is why the shoulder deformity

was not addressed in childhood at the time of the cleft

lip and cleft palate repair. A similar scenario has been

reported before from Japan (14). Had the Sprengel

deformity been repaired in childhood it is possible the

outcome would have been better then. Earlier in the

postoperative period there were indications that the

range of shoulder movement had improved. As of the

last review, the patient did not have an unsightly scar

but there still persisted a disparity of the levels of the

scapulae.

REFERENCES

1. DePalma, Anthony F. Surgery of the shoulder. 3rd Edition. J.B.lippincott. Philadelphia. 1983.pg 24-25.

2. Tachdjian MO. Congenital High Scapula (Sprengel’s Deformity). In Tachdjians Paediatric Orthopaedics. Vol 1. 2nd Edition. 1990. Philadelphia. WB Saunders. pg 136-168

3. Woodward, J. W. Congenital Elevation of the Scapula.J. Bone Joint Surg. AM. 1961. 43A.2.219-228

4. Boon JM: Potgieter D: Van Jaarsveld Z et al. Congential Undescended Scapula (Sprengel Deformity): A case study. Clinical Anatomy.2002.15.139-142

5. Dilli A, Ayaz, U. Y., Damar, C., et al. Sprengel Deformity: Magnetic Resonance Imaging Findings in two Pediatric Cases. Journal of Clinical Imaging Sci. 2011. 1. 1. 17-20

6. Cavendish, M. E. Congenital Elevation of the Scapula. J. Bone joint Surg. Br. 1972. 54B. 3.395-408

7. Green, W. T. The surgical correction of congenital elevation of the scapula (Sprengel’s deformity). Journal of Bone and Joint Surgery AM. 1957. 39A. 6.1439.

8. Grogan, D. P., Stanley, E. A. and Bobechko, W. P. The Congenital undescended scapula. Journal of Bone and joint Surgery.Br.1983. 65B. 5. 598-605.

9. Ross, D. M. and Cruess, R. L. The Surgical Correction of Congenital Elevation of the Scapula. Clinical Orthopaedics Related Research.1977.125.17-23.

10. Cho, T. J., Choi, I. H., Chung, C. Y., et al. The Sprengel deformity: Morphometric analysis using 3D-CT and its clinical relevance. Journal of Bone and Joint Surgery.Br. 2000. 82B. 5. 711-718

11. Petrie, J. G. Congenital elevation of the scapula. Journal of Bone and Joint Surgery-BR. 1973. 55B. 441

12. Le Saout, J. Congenital elevation of the scapula (Sprengel’s deformity) In Professor Jacques Duparc (Ed) EFORT Surgical Techniques In Orthopaedics and Traumatology. Elsevier 2003. pg 55-210-C-10

13. Leibovic, S. J., Ehrlich, M. E. and Zaleske, D. J. Sprengel deformity. Journal of Bone and Joint Surgery.Am. 1990. 72A. 2. 192-197

14. Doita, M., Lio, H. and Mizuno, K. Surgical Management of Sprengel’s Deformity in Adults. Clinical Orthopaedics Related Research. 2000. 371. 119-124.

15. Carson, W. G., Lovell, W. W. and Whitesides, T. E. Congenital Elevation of the Scapula. Journal of Bone and Joint Surgery.AM. 1981. 63A. 8. 1199-1207.

16. Siu, K. K., Ko, J. Y., Huang, C. C., et al. Woodward Procedure Improves Shoulder Function In Sprengel Deformity. Chang Gung Medical Journal. 2011. 34. 4. 403-408

17. Ahmad, A. A. Surgical Correction of Severe Sprengel deformity to allow greater postoperative range of Shoulder abduction. Journal of Paediatric Orthopaedics. 2010. 30. 6. 575-581

18. Borges, J. L., Shah, A., Torres, B. C., et al. Modified Woodward procedure for Sprengel deformity of the Shoulder: Long –term results. J. Paed. Orthopaed. 1996. 16. 508-513

19. Gonen, E., Simsek, U., Solak, S., et al. Long-Term Results of Modified Green Method in Sprengel’s Deformity. J. Children Orthopaedics. 2010. 4. 309-314.

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19. Gonen, E., Simsek,U., Solak, S., et al. Long-term results of modified green method in Sprengel’s deformity. J. Children Orthopaed. 2010; 4: 309-314.