Cutis laxa with growth and developmental delay
| dc.authorid | 113274 | en_US |
| dc.contributor.author | Karakurt, Cemşit | |
| dc.contributor.author | Sipahi, T. | |
| dc.contributor.author | Ceylaner, S. | |
| dc.contributor.author | Şenocak, Filiz | |
| dc.contributor.author | Karademir, Selmin | |
| dc.contributor.author | Becer, M. | |
| dc.date.accessioned | 2018-01-30T10:10:13Z | |
| dc.date.available | 2018-01-30T10:10:13Z | |
| dc.date.issued | 2001 | |
| dc.department | İnönü Üniversitesi | en_US |
| dc.description | Clinical Pediatrics. | en_US |
| dc.description.abstract | Congenital cutis laxa is a rare inherited disorder of connective tissue manifested by loose, hanging skin. Cutis laxa may be inherited (autosomal dominant, autosomal recessive) or acquired. As opposed to the recessive form of cutis laxa, the dominant form has been reported to be free of pulmonary and other internal manifestation.' Skin fibroblast cultures from cutis laxa patients exhibit reduced elastin. The genetic map locus of autosomal dominant form is 7q11.2. Tassabehji et a12 have described patients with autosomal dominant cutis laxa and mutations in elastin gene. | en_US |
| dc.identifier.citation | Karakurt C., Sipahi T, Ceylaner S., Senocak F, Karademir S., Becer M. (2001). Cutis laxa with growth and developmental delay. Clinical Pediatrics. | en_US |
| dc.identifier.doi | 10.1177/000992280104000715 | en_US |
| dc.identifier.endpage | 0 | en_US |
| dc.identifier.issue | 0 | en_US |
| dc.identifier.startpage | 0 | en_US |
| dc.identifier.uri | http://journals.sagepub.com/doi/pdf/10.1177/000992280104000715 | |
| dc.identifier.uri | https://hdl.handle.net/11616/8029 | |
| dc.identifier.volume | 0 | en_US |
| dc.language.iso | en | en_US |
| dc.publisher | Clinical Pediatrics | en_US |
| dc.relation.ispartof | Clinical Pediatrics | en_US |
| dc.rights | info:eu-repo/semantics/openAccess | en_US |
| dc.title | Cutis laxa with growth and developmental delay | en_US |
| dc.type | Article | en_US |
