Literature DB >> 17664768

Progeria (Hutchison-Gilford syndrome) in siblings: in an autosomal recessive pattern of inheritance.

T Y Raghu1, G A Venkatesulu, G R Kantharaj, T Suresh, V Veeresh, Y Hanumanthappa.   

Abstract

Progeria 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.

Entities:  

Year:  2001        PMID: 17664768

Source DB:  PubMed          Journal:  Indian J Dermatol Venereol Leprol        ISSN: 0378-6323            Impact factor:   2.545


  1 in total

1.  Progeria in siblings: a rare case report.

Authors:  R Sowmiya; D Prabhavathy; S Jayakumar
Journal:  Indian J Dermatol       Date:  2011 Sep-Oct       Impact factor: 1.494

  1 in total

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