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Congenital cutis laxa syndrome: type II autosomal recessive inheritance

Cutis laxa is a term that refers to markedly loose skin that is not hyperelastic. It is regarded as a genetically heterogeneous group of diseases and is presently divided into five types. We report a male patient with type II autosomal recessive disease. The patient was the third child of fir...

תיאור מלא

שמור ב:
מידע ביבליוגרפי
Principais autores: Beyhan Tüysüz, Müjde Arapoğlu, Barbaros Ilikkan, Cuyan Demirkesen, Yildiz Perk
פורמט: Artigo
שפה:Inglês
יצא לאור: Hacettepe University Institute of Child Health 2003-07-01
סדרה:The Turkish Journal of Pediatrics
גישה מקוונת:https://turkjpediatr.org/article/view/2902
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