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53 Possible Causes for Iridocorneal Dysgenesis

  • Blepharitis

    To report the association of Kaposi varicelliform eruption (KVE) with 0.1% tacrolimus ointment treatment of atopic blepharitis in a patient with atopic dermatitis (AD). We encountered KVE in a 20-year-old male patient with atopic blepharitis and AD who developed generalized herpetic lesions on his face 28 days after[…][ncbi.nlm.nih.gov]

  • Iridocorneal Dysgenesis

    Iridocorneal dysgenesis • Axenfeld-Rieger anomaly • Peters anomaly • Aniridia • Sturge-Weber syndrome • Neurofibromatosis - 1 Page 2 CONGENITAL GLAUCOMAS 1. Primary 3.[edurev.in] Search dictionary help iridocorneal mesodermal dysgenesis medical dictionary Mesodermal dysgenesis of cornea and iris , producing pupillary anomalies , posterior embryotoxon[mondofacto.com] We have recently studied four generations of the family of a child with frank iridocorneal mesodermal dysgenesis.[healio.com]

  • Secondary Glaucoma

    dysgenesis.[emedicine.medscape.com] Iridocorneal dysgenesis - this can arise in a number of conditions (Axenfeld-Rieger syndrome, Peters' anomaly, aniridia) and is variously associated with glaucoma, the management[patient.info] Numerous iris processes and iridocorneal adhesions could be seen in these diseases. Neovascular glaucoma has been reported in Stickler syndrome.[emedicine.medscape.com]

  • Congenital Microcoria

    The identification of a null GPR180 mutation segregating over two generations with iridocorneal angle dysgenesis, which can be regarded as a MCOR endophenotype, is consistent[ncbi.nlm.nih.gov]

  • Iris Atrophy

    The differential diagnosis of multiple iris nodules includes neurofibromatosis, melanomas, inflammatory nodules, and developmental anomalies such as iridocorneal dysgenesis[ncbi.nlm.nih.gov]

  • Warburg Sjo Fledelius Syndrome

    Sentences Mobile Microcornea and iridocorneal dysgenesis also occur. "' Micro syndrome "'also known as WARBM, and Warburg Sjo Fledelius syndrome, is a rare autosomal recessive[eng.ichacha.net]

  • Congenital Cataract - Microcornea - Corneal Opacity

    To investigate whether three consanguineous families from the Punjab province of Pakistan, with affected members with recessively inherited congenital cataract microcornea with corneal opacity, are genetically homogeneous. An ophthalmic examination was performed on each family member to establish the diagnosis. The[…][ncbi.nlm.nih.gov]

  • Axenfeld Anomaly

    Iridocorneal dysgenesis Correct answer : D.[pgblazer.com] Iridocorneal dysgenesis with glaucoma. In: Epstein DL (eds) Chandler and Grant’s Glaucoma , 3rd ed, Chap 38.[nature.com] Axenfeld anomaly is seen in glaucoma associated with iridocorneal dysgenesis. It is a posterior embryotoxon characterised by prominent Schwalbe’s ring.[pgblazer.com]

  • Glaucoma

    Iridocorneal dysgenesis - this can arise in a number of conditions (Axenfeld-Rieger syndrome, Peters' anomaly, aniridia) and is variously associated with glaucoma, the management[patient.info]

  • Rieger Syndrome

    Synonym(s): iridocorneal mesodermal dysgenesis Rieger syndrome - Rieger anomaly combined with hypodontia or anodontia and maxillary hypoplasia.[medical-dictionary.thefreedictionary.com] Other authors prefer the umbrella terms of anterior segment dysgenesis or iridocorneal dysgenesis. Clinical findings are bilateral, but often asymmetric.[webeye.ophth.uiowa.edu] Rie·ger syn·drome ( rē'ger sin'drōm ) [MIM*180500] Iridocorneal mesenchymal dysgenesis combined with hypodontia or anodontia and maxillary hypoplasia.[medical-dictionary.thefreedictionary.com]

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