Unusual presentation of Norrie's disease with hypomagnesemia.

Kumar, M S; Shenoi, A; Mukta Jain, M; Ashok, J; Chidananda, S C; Sameera, P; Maseeuddin, S

Kumar, M S; Shenoi, A; Mukta Jain, M; Ashok, J; Chidananda, S C; Sameera, P; Maseeuddin, S.

Indian Pediatr ; 1998 Aug; 35(8): 783-6

Article in English | IMSEAR | ID: sea-9887

Subject(s)

Atrophy; Blindness/congenital; Brain/pathology; Consanguinity; Deafness/congenital; Humans; Infant; Genetic Linkage/genetics; Magnesium/blood; Male; Intellectual Disability/genetics; Microphthalmos/genetics; Retinal Detachment/congenital; Vitreous Body/abnormalities; X Chromosome/genetics

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Full text: Available Index: IMSEAR (South-East Asia) Main subject: Atrophy / Vitreous Body / X Chromosome / Brain / Retinal Detachment / Humans / Male / Microphthalmos / Blindness / Consanguinity Language: English Journal: Indian Pediatr Year: 1998 Type: Article

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