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, sa.3, ss.265-268, 2003 (SCI-Expanded) identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 45 Sayı: 3
  • Basım Tarihi: 2003
  • Dergi Adı: TURKISH JOURNAL OF PEDIATRICS
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.265-268
  • İstanbul Üniversitesi Adresli: Evet

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.