Congetial cutis laxa syndrome: type II autosomal recessive inheritance


Tuysuz B. , ARAPOGLU M., ILIKKAN B. , DEMIRKESEN C. , PERK Y.

TURKISH JOURNAL OF PEDIATRICS, cilt.45, ss.265-268, 2003 (SCI İndekslerine Giren Dergi)

  • Cilt numarası: 45 Konu: 3
  • Basım Tarihi: 2003
  • Dergi Adı: TURKISH JOURNAL OF PEDIATRICS
  • Sayfa Sayısı: ss.265-268

Özet

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 H autosomal recessive disease.