Literature DB >> 17642895

Familial acrogeria in a brother and sister.

S M Ahmad1, I Majeed.   

Abstract

Acrogeria is one of the premature aging syndromes with an unknown mode of inheritance. Familial cases are quite rare. A report of the disease in a brother and sister demonstrating a possible autosomal recessive inheritance is described. An unusual finding was bilateral corneal opacities in both the patients.

Entities:  

Year:  2003        PMID: 17642895

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


  1 in total

1.  A rare case of acrogeria.

Authors:  Sunil Sanghi; R S Grewal; Biju Vasudevan; A Nagure
Journal:  Med J Armed Forces India       Date:  2013-04-08
  1 in total

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