Neonatal Features of the Prader-Willi Syndrome; The Case for Making the Diagnosis During the First Week of Life

Cizmecioglu, FİLİZ; Jones, Jeremy; Paterson, Wendy; Kherra, Sakina; Kourime, Mariam; McGowan, Ruth; Shaikh, M.; Donaldson, Malcolm

doi:10.4274/jcrpe.0029

Neonatal Features of the Prader-Willi Syndrome; The Case for Making the Diagnosis During the First Week of Life

Atıf İçin Kopyala

Cizmecioglu F. M. , Jones J. H. , Paterson W. F. , Kherra S., Kourime M., McGowan R., et al.

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY, cilt.10, ss.264-273, 2018 (SCI İndekslerine Giren Dergi)

Cilt numarası: 10 Konu: 3
Basım Tarihi: 2018
Doi Numarası: 10.4274/jcrpe.0029
Dergi Adı: JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY
Sayfa Sayısı: ss.264-273

Özet

Objective: Early diagnosis is of proven benefit in Prader-Willi syndrome (PWS). We therefore examined key perinatal features to aid early recognition.