PRENATAL DÖNEMDE TANI KOYULAN İZOLE YARIK EL/ AYAK MALFORMASYONU


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İstanbul Üniversitesi İstanbul Tıp Fakültesi Mecmuası, vol.81, no.1, pp.37-41, 2018 (National Refreed University Journal)

  • Publication Type: Article / Case Report
  • Volume: 81 Issue: 1
  • Publication Date: 2018
  • Doi Number: 10.18017/iuitfd.375085
  • Title of Journal : İstanbul Üniversitesi İstanbul Tıp Fakültesi Mecmuası
  • Page Numbers: pp.37-41

Abstract

ÖÖDDtkilenen ekstremitede me-
dial yarıklar, sindaktili ve falanks, metakarp ve metatarslarda hipoplazi ve/veya aplazi ile kendini gösterir. İzole bir anomali
olabileceği gibi çeşitli anomalilerle birliktelik gösterek bir sendromun parçası olabilir. Bu makalede 27 haftada kliniği
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 accom
-
pany a syndrome. İn 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