Walker–Warburg syndrome
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Walker–Warburg syndrome (WWS), also called Warburg syndrome, Chemke syndrome, HARD syndrome (Hydrocephalus, Agyria and Retinal Dysplasia), Pagon syndrome, cerebroocular dysgenesis (COD) or cerebroocular dysplasia-muscular dystrophy syndrome (COD-MD),[1] is a rare form of autosomal recessive congenital muscular dystrophy.[2] It is associated with brain (lissencephaly, hydrocephalus, cerebellar malformations) and eye abnormalities.[3] This condition has a worldwide distribution. Walker-Warburg syndrome is estimated to affect 1 in 60,500 newborns worldwide.[4]
Quick Facts Other names, Specialty ...
Walker–Warburg syndrome | |
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Other names | HARD syndrome,Warburg syndrome |
Walker–Warburg syndrome has an autosomal recessive pattern of inheritance. | |
Specialty | Ophthalmology, neurology, medical genetics |
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