Yazar "Aydın, Elif Nazlı Çetindağ" için listeleme
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Recurrent Case of a Rare and Devastating Entity: Harlequin Ichthyosis
Harlequin ichthyosis (HI) is a rare and severe form of congenital ichthyosis caused by truncating mutations in the ABCA12 gene. Although it has many distinctive signs on perinatal sonography such as short limbs, wide gaping ...