| dc.contributor.author | Kılıç, Fatma Arzu | |
| dc.contributor.author | Çakmak, Seray Kulcu | |
| dc.contributor.author | Tuncalı, Timur | |
| dc.contributor.author | Koz, Özlem | |
| dc.contributor.author | Özhamamci, Esra | |
| dc.contributor.author | Yasun, Oztan | |
| dc.contributor.author | Artuz, Ferda | |
| dc.date.accessioned | 2019-10-28T06:03:32Z | |
| dc.date.available | 2019-10-28T06:03:32Z | |
| dc.date.issued | 2015 | en_US |
| dc.identifier.issn | 1642-395X | |
| dc.identifier.uri | https://doi.org/10.5114/pdia.2015.56102 | |
| dc.identifier.uri | https://hdl.handle.net/20.500.12462/9291 | |
| dc.description | Kılıç, Fatma Arzu (Balikesir Author) | en_US |
| dc.description.abstract | Seckel syndrome (SCKL) is an extremely rare form of
primordial dwarfism characterized by growth delay, proportionate extreme short stature, a prominent beak-like
nose, hypoplasia of the malar area, small chin, microcephaly, and skeletal malformations [1–4]. In this review,
two siblings with a combination of clinical, skeletal, ocular, dental and cytogenetic findings are presented in view
of SCKL | en_US |
| dc.language.iso | eng | en_US |
| dc.publisher | Termedia Publishing House Ltd | en_US |
| dc.relation.isversionof | 10.5114/pdia.2015.56102 | en_US |
| dc.rights | info:eu-repo/semantics/openAccess | en_US |
| dc.title | Seckel syndrome with cutaneous pigmentary changes: two siblings and a review of the literature | en_US |
| dc.type | other | en_US |
| dc.relation.journal | Postepy Dermatologii I Alergologii | en_US |
| dc.contributor.department | Tıp Fakültesi | en_US |
| dc.contributor.authorID | 0000-0003-2 983-065X | en_US |
| dc.identifier.volume | 32 | en_US |
| dc.identifier.issue | 6 | en_US |
| dc.identifier.startpage | 470 | en_US |
| dc.identifier.endpage | 474 | en_US |
| dc.relation.publicationcategory | Diğer | en_US |
