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Congetial cutis laxa syndrome: type II autosomal recessive inheritance

dc.contributor.authorTuysuz, Beyhan
dc.contributor.authorILIKKAN, Barbaros
dc.contributor.authorPERK, Yıldız
dc.contributor.authorDEMIRKESEN, Cüyan
dc.contributor.authorARAPOGLU, M
dc.date.accessioned2021-03-04T13:23:08Z
dc.date.available2021-03-04T13:23:08Z
dc.date.issued2003
dc.identifier.citationTuysuz B., ARAPOGLU M., ILIKKAN B., DEMIRKESEN C., PERK Y., "Congetial cutis laxa syndrome: type II autosomal recessive inheritance", TURKISH JOURNAL OF PEDIATRICS, cilt.45, sa.3, ss.265-268, 2003
dc.identifier.issn0041-4301
dc.identifier.othervv_1032021
dc.identifier.otherav_7c2e5fcd-8b3e-405b-96af-fea495efc893
dc.identifier.urihttp://hdl.handle.net/20.500.12627/84930
dc.description.abstractCutis 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.
dc.language.isoeng
dc.subjectTıp
dc.subjectÇocuk Sağlığı ve Hastalıkları
dc.subjectSağlık Bilimleri
dc.subjectDahili Tıp Bilimleri
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectPEDİATRİ
dc.titleCongetial cutis laxa syndrome: type II autosomal recessive inheritance
dc.typeMakale
dc.relation.journalTURKISH JOURNAL OF PEDIATRICS
dc.contributor.department, ,
dc.identifier.volume45
dc.identifier.issue3
dc.identifier.startpage265
dc.identifier.endpage268
dc.contributor.firstauthorID9862


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