Kocher Debre Semelaigne syndrome (case report).

Agrawal, B V; Kumar, V; Misr, S K; Vaish, S K; Rastogi, B L; Bajpai, H S

Agrawal, B V; Kumar, V; Misr, S K; Vaish, S K; Rastogi, B L; Bajpai, H S.

Article in English | IMSEAR | ID: sea-86102

Subject(s)

Child; Congenital Hypothyroidism/complications; Humans; Hypertrophy/pathology; Hypothyroidism/complications; Male; Muscular Diseases/complications; Syndrome

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Full text: Available Index: IMSEAR (South-East Asia) Main subject: Syndrome / Humans / Male / Child / Congenital Hypothyroidism / Hypertrophy / Hypothyroidism / Muscular Diseases Language: English Year: 1979 Type: Article

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