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dc.contributor.authorYuksel, Atil
dc.contributor.authorAltunoglu, Umut
dc.contributor.authorTurkyilmaz, Gurcan
dc.contributor.authorHas, Recep
dc.contributor.authorKalelioglu, Ibrahim
dc.contributor.authorAvci, Sahin
dc.contributor.authorSarac Sivrikoz, Tugba
dc.contributor.authorErturk, Emircan
dc.date.accessioned2021-03-04T11:57:48Z
dc.date.available2021-03-04T11:57:48Z
dc.date.issued2018
dc.identifier.citationTurkyilmaz G., Avci S., Erturk E., Sarac Sivrikoz T., Altunoglu U., Kalelioglu I., Has R., Yuksel A., "PRENATAL DIAGNOSIS OF ISOLATED SPLIT HAND/FOOT MALFORMATION", JOURNAL OF ISTANBUL FACULTY OF MEDICINE-ISTANBUL TIP FAKULTESI DERGISI, cilt.81, sa.1, ss.37-41, 2018
dc.identifier.othervv_1032021
dc.identifier.otherav_74f2e23d-bfec-4a58-801c-658a8687d741
dc.identifier.urihttp://hdl.handle.net/20.500.12627/80368
dc.description.abstractSplit hand/foot malformation (SHFM) also known ectrodactyly is a rare orthopaedic malformation which is characterised by the deficiency or absence of one or more central digits of the hand or foot. The associated anomalies are median cleft, syndactyly or aplasia/hypoplasia of the phalanges, metacarpals and metatarsals of hands or feet. It can be isolated or accompany a syndrome. In our case, we introduced prental diagnosis of isolated form of ectrodactyly in both extremities. After genetic counselling we terminated the. In this report, we aimed to explain the importance of multidiciplinary approach to extremity anomalies.
dc.language.isoeng
dc.subjectTıp
dc.subjectTemel Tıp Bilimleri
dc.subjectSağlık Bilimleri
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectTIP, GENEL & İÇECEK
dc.titlePRENATAL DIAGNOSIS OF ISOLATED SPLIT HAND/FOOT MALFORMATION
dc.typeMakale
dc.relation.journalJOURNAL OF ISTANBUL FACULTY OF MEDICINE-ISTANBUL TIP FAKULTESI DERGISI
dc.contributor.department, ,
dc.identifier.volume81
dc.identifier.issue1
dc.identifier.startpage37
dc.identifier.endpage41
dc.contributor.firstauthorID248311


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