Yazar "Yildirim, Mehmet E. C." seçeneğine göre listele

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  • Küçük Resim Yok
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    A rare case of gestational gigantomastia
    (Wiley, 2019) Karacor-Altuntas, Zeynep; Yildirim, Mehmet E. C.; Findik, Sidika
    [Abstract Not Availabe]
  • Küçük Resim Yok
    Öğe
    Variable expression of Van der Woude syndrome: A case report
    (Wiley, 2020) Altuntas, Zeynep; Ismayilzade, Majid; Altuntas, Mahmut; Yildirim, Mehmet E. C.
    Van der Woude syndrome (VWS) is an autosomal dominant disorder with a rare clinical manifestation of orofacial disorders with deletion in the 1q32-q41 chromosome band. In our study we present a clinical case of a 1-year old boy with a bilateral cleft lip, a cleft palate and bilateral congenital pits on the lower lip and a father with various clinical presentations of VWS.