Browsing by Author "Kantharaj, G R"
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Item Dyschromatosis universalis: autosomal dominant pattern.(2002-01-28) Kantharaj, G R; Siddalingappa, K; Chidambara, Murthy SItem Hereditary sensory autonomic neuropathy--type II in siblings.(1996-10-01) Balachandran, C; Sabitha, L; Kantharaj, G RItem Progeria (Hutchison-Gilford syndrome) in siblings: in an autosomal recessive pattern of inheritance.(2001-09-01) Raghu, T Y; Venkatesulu, G A; Kantharaj, G R; Suresh, T; Veeresh, V; Hanumanthappa, YProgeria is an autosomal dominant, premature aging syndrome. Six and three year old female siblings had sclerodermatous changes over the extremities, alopecia, beaked nose, prominent veins and bird-like facies. Radiological features were consistent with features of progeria. The present case highlights rarity of progeria in siblings with a possible autosomal recessive pattern.