congenital glaucomas

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CONGENITAL GLAUCOMAS 1. Primary 3. In phacomatoses 2. Iridocorneal dysgenesis Axenfeld-Rieger anomaly Peters anomaly Aniridia Sturge-Weber syndrome Neurofibromatosis - 1

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CONGENITAL GLAUCOMAS. 1. Primary. 2. Iridocorneal dysgenesis. Axenfeld-Rieger anomaly. Peters anomaly. Aniridia. 3. In phacomatoses. Sturge-Weber syndrome. Neurofibromatosis - 1. Primary congenital glaucoma. 1:10,000 births, 65% boys. - PowerPoint PPT Presentation

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Page 1: CONGENITAL GLAUCOMAS

CONGENITAL GLAUCOMAS

1. Primary

3. In phacomatoses

2. Iridocorneal dysgenesis• Axenfeld-Rieger anomaly• Peters anomaly• Aniridia

• Sturge-Weber syndrome• Neurofibromatosis - 1

Page 2: CONGENITAL GLAUCOMAS

Primary congenital glaucoma• 1:10,000 births, 65% boys• Most sporadic - 10% autosomal recessive

Flat iris insertion Concave iris insertion

• Absence of angle recess with iris inserted directly into trabeculum

Page 3: CONGENITAL GLAUCOMAS

Clinical features of primary congenital glaucoma

Breaks in Descemet membrane

• Depend on age of onset• Bilateral in 75% but frequently asymmetrical

Corneal oedema associated with lacrimation and photophobia

Buphthalmos if IOP becomes elevated prior to age 3 years.

Optic disc cupping

Page 4: CONGENITAL GLAUCOMAS

Management of primary congenital glaucoma

Goniotomy TrabeculotomyMeasurement of IOP and corneal diameters

Page 5: CONGENITAL GLAUCOMAS

Axenfeld anomaly• Bilateral but asymmetrical• Glaucoma is uncommon

Posterior embryotoxon Attached strands of iris to posterior embryotoxon

Page 6: CONGENITAL GLAUCOMAS

Rieger anomaly• Autosomal dominant• Bilateral but asymmetrical

Stromal hypoplasia and corectopia Ectropion uveae

Full-thickness iris atrophy Angle anomalies

• Glaucoma in 50%

Page 7: CONGENITAL GLAUCOMAS

Rieger syndrome

Rieger anomaly Dental and facial anomalies

Page 8: CONGENITAL GLAUCOMAS

Peters anomaly• Usually sporadic

• Glaucoma in 50%

Corneal opacity with iris adhesions

• Bilateral in 80%

Corneal opacity with lenticular adhesions

Page 9: CONGENITAL GLAUCOMAS

Systemic Implications of Aniridia

• Autosomal dominantAN-1 - 85%

• Isolated

AN-2 (Miller syndrome) - 13%

• Deletion of short arm of chromosome 11• Wilm tumour, genitourinary anomalies and mental handicap

• Autosomal recessive• Mental handicap and cerebellar ataxia

AN-3 (Gillespie syndrome) - 2%

Page 10: CONGENITAL GLAUCOMAS

Signs of aniridia

Subtotal absence

Synechial angle-closureglaucoma in 75%

Occasional cataract and lenssubluxation

Partial absence

Page 11: CONGENITAL GLAUCOMAS

Glaucoma in Sturge-Weber syndrome

• Glaucoma in 30%• Ipsilateral to facial haemangioma• Buphthalmos in 60%

• Caused by raised episcleral venous pressure associated with episcleral haemangioma• Angle anomaly may also be responsible

Glaucoma Causes

Page 12: CONGENITAL GLAUCOMAS

Glaucoma in neurofibromatosis - 1

• Glaucoma is ipsilateral to neurofibroma of upper eyelid in 50% of cases

• Caused by angle anomaly with or without ectropion uveae• Angle neurofibroma may also be responsible

Glaucoma Causes