Please use this identifier to cite or link to this item: https://hdl.handle.net/11499/4431
Full metadata record
DC FieldValueLanguage
dc.contributor.authorErgin, Hacer-
dc.contributor.authorSemerci, Cavidan Nur-
dc.contributor.authorBican, M.-
dc.contributor.authorDüzcan, Füsun-
dc.contributor.authorYagci, A.B.-
dc.contributor.authorErdogan, K.M.-
dc.contributor.authorTufan, Ahmet Çevik-
dc.date.accessioned2019-08-16T11:34:03Z-
dc.date.available2019-08-16T11:34:03Z-
dc.date.issued2006-
dc.identifier.issn0041-4301-
dc.identifier.urihttps://hdl.handle.net/11499/4431-
dc.description.abstractMalformations of the lower limbs are rare and heterogeneous anomalies. Some congenital anomalies involving face, gastrointestinal system, skeletal system, urogenital system, heart, lung and diaphragma associated with lower limb malformations have been described in the literature. Here, we report a case of left proximal femoral focal deficiency (PFFD) together with fibular aplasia associated with left undescended testis and hypospadias. The putative embryologic mechanisms of lower limb defects and their possible association with lower urogenital tract malformations are also discussed.en_US
dc.language.isoenen_US
dc.relation.ispartofTurkish Journal of Pediatricsen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectFibular a/hypoplasia (FA/H)en_US
dc.subjectHox genesen_US
dc.subjectProximal femoral focal deficiency (PFFD)en_US
dc.subjectUrogenital anomaliesen_US
dc.subjectarticleen_US
dc.subjectbirth weighten_US
dc.subjectbody heighten_US
dc.subjectbone radiographyen_US
dc.subjectcase reporten_US
dc.subjectchromosome analysisen_US
dc.subjectcryptorchismen_US
dc.subjectdisease associationen_US
dc.subjectembryo developmenten_US
dc.subjectfibula aplasiaen_US
dc.subjectfoot radiographyen_US
dc.subjectgestational ageen_US
dc.subjecthumanen_US
dc.subjecthypospadiasen_US
dc.subjectinfanten_US
dc.subjectleg malformationen_US
dc.subjectmaleen_US
dc.subjectphysical examinationen_US
dc.subjectproximal femoral focal deficiencyen_US
dc.subjectsyndactylyen_US
dc.subjecturogenital tract malformationen_US
dc.subjectAbnormalities, Multipleen_US
dc.subjectCryptorchidismen_US
dc.subjectEctromeliaen_US
dc.subjectFemuren_US
dc.subjectFibulaen_US
dc.subjectGenes, Homeoboxen_US
dc.subjectHomeodomain Proteinsen_US
dc.subjectHumansen_US
dc.subjectHypospadiasen_US
dc.subjectInfant, Newbornen_US
dc.subjectKaryotypingen_US
dc.subjectMaleen_US
dc.subjectMutationen_US
dc.titleA case with proximal femoral focal deficiency (PFFD) and fibular A/hypoplasia (FA/H) associated with urogenital anomaliesen_US
dc.typeArticleen_US
dc.identifier.volume48en_US
dc.identifier.issue4en_US
dc.identifier.startpage380-
dc.identifier.startpage380en_US
dc.identifier.endpage382en_US
dc.authorid0000-0001-5287-8526-
dc.authorid0000-0002-3973-1404-
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.identifier.pmid17290579en_US
dc.identifier.scopus2-s2.0-33846104916en_US
dc.identifier.wosWOS:000243778900020en_US
dc.identifier.scopusqualityQ3-
dc.ownerPamukkale_University-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.grantfulltextnone-
item.languageiso639-1en-
item.openairetypeArticle-
item.fulltextNo Fulltext-
item.cerifentitytypePublications-
crisitem.author.dept14.02. Internal Medicine-
crisitem.author.dept14.02. Internal Medicine-
crisitem.author.dept14.02. Internal Medicine-
crisitem.author.dept14.03. Basic Medical Sciences-
Appears in Collections:PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection
Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
Tıp Fakültesi Koleksiyonu
WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection
Show simple item record



CORE Recommender

SCOPUSTM   
Citations

4
checked on Dec 14, 2024

WEB OF SCIENCETM
Citations

4
checked on Dec 20, 2024

Page view(s)

74
checked on Aug 24, 2024

Google ScholarTM

Check





Items in GCRIS Repository are protected by copyright, with all rights reserved, unless otherwise indicated.