| Literature DB >> 17642895 |
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