Literature DB >> 11321244

Restrictive dermopathy: case report, subject review with Kaplan-Meier analysis, and differential diagnosis of the lethal congenital contractural syndromes.

C Sergi1, J Poeschl, M Graf, O Linderkamp.   

Abstract

We report on a 34-week-old infant with restrictive dermopathy (RD), a rare lethal genodermatosis, characterized by an abnormal skin growth and differentiation with thin, tightly adherent skin that causes a dysmorphic face, generalized flexion joint contractures, and respiratory insufficiency. Kaplan-Meier analysis of 32 previously well-described infants affected with RD showed a median survival of 132 hours. Lethal congenital contractural syndromes, including Pena-Shokeir phenotype, cerebro-oculo facio-skeletal syndrome, and lethal multiple pterygium syndrome, should be considered first in the differential diagnosis. Other lethal contractural syndromes are discussed.

Entities:  

Mesh:

Year:  2001        PMID: 11321244     DOI: 10.1055/s-2001-12938

Source DB:  PubMed          Journal:  Am J Perinatol        ISSN: 0735-1631            Impact factor:   1.862


  1 in total

1.  Mice with targeted disruption of the fatty acid transport protein 4 (Fatp 4, Slc27a4) gene show features of lethal restrictive dermopathy.

Authors:  Thomas Herrmann; Frank van der Hoeven; Hermann-Josef Grone; Adrian Francis Stewart; Lutz Langbein; Iris Kaiser; Gerhard Liebisch; Isabella Gosch; Florian Buchkremer; Wolfgang Drobnik; Gerd Schmitz; Wolfgang Stremmel
Journal:  J Cell Biol       Date:  2003-06-23       Impact factor: 10.539

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.