Literature DB >> 881093

Acrogeria. A case report.

A Hjortshoj, G Heydenreich.   

Abstract

A case of acrogeria in a 12-year-old girl is reported. Acrogeria is a rare, nonhereditary, probably congenital disease of which the main characteristic is an atrophy of the skin giving it an aged appearance. The defect is localized to the dermis and subcutis, whereas, the epidermis seems not to be affected. The disease might be associated with other congenital malformations.

Entities:  

Mesh:

Year:  1977        PMID: 881093

Source DB:  PubMed          Journal:  Dermatologica        ISSN: 0011-9075


  3 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

2.  Skeletal abnormalities of acrogeria, a progeroid syndrome.

Authors:  A Ho; S J White; J E Rasmussen
Journal:  Skeletal Radiol       Date:  1987       Impact factor: 2.199

Review 3.  Gottron's acrogeria and sarcoidosis.

Authors:  A Meurer; G Lohmöller; C Keller
Journal:  Clin Investig       Date:  1993-05
  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.