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Anterior segment dysgenesis

MONDO:0019503

A spectrum of developmental anomalies that affect the development of the anterior segment of the eyeball resulting from abnormalities of neural crest migration and differentiation during embryologic development (Axenfeld-Rieger syndrome, Peters anomaly, posterior keratoconus, and iridoschisis).

Also known as: ASGD, ASMD, ASOD, anterior segment mesenchymal dysgenesis, anterior segment ocular dysgenesis, familial ocular anterior segment mesenchymal dysgenesis

27 clinical trials for this condition and its sub-types.

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Sub-types

Congenital primary aphakia (14) Anterior segment dysgenesis 1 (1) Anterior segment dysgenesis 6 (1) Axenfeld-Rieger syndrome type 3 (1) Congenital microcoria (1) Peters anomaly (1) Aniridia-cerebellar ataxia-intellectual disability syndrome (0) Anterior segment dysgenesis 3 (0) Anterior segment dysgenesis 4 (0) Anterior segment dysgenesis 7 (0) Anterior segment dysgenesis 8 (0) Bilateral acute depigmentation of the iris (0) Chromosome 6pter-p24 deletion syndrome (0) Congenital ectropion uveae (0) FOXC1-related anterior segment dysgenesis (0) Iridogoniodysgenesis (0) Isolated iridoschisis (0) Peters anomaly-cataract syndrome (0) Rieger anomaly (0) Von Hippel anomaly (0)

Broader categories

Disease (618) Hereditary disease (172) Eye disorder (97) Human disease (14) Disorder of orbital region (3) Disease of genetic or genomic mechanism (2) Disorder of visual system (1) Disease by body system or component (0) Disease by developmental or physiological process (0) Disease by etiologic mechanism (0)
Trials to join now! 13 Not yet recruiting 3 Not yet finished but already full! 5 Completed 5 Terminated 1
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