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PedAM

Pediatric Disease Annotations & Medicines




Disease cataract
Symptom C1510497|lens opacities
Sentences 2
PubMedID- 21836522 Results: in one family, a novel bfsp2 mutation causes autosomal recessive diffuse cortical cataract with scattered lens opacities, and in another, a novel pitx3 mutation causes an autosomal recessive severe form of anterior segment dysgenesis and microphthalmia.
PubMedID- 25002996 He had bilateral cataract with punctate lens opacities.

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