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Congenital portosystemic shunt in a child with Wolf–Hirschhorn syndrome

✍ Scribed by Hiroshi Koga; Kenichi Miyako; Yoshihiro Sakemi; Tomoko Hidaka; Naohiro Suga; Noboru Takahashi

Publisher
John Wiley and Sons
Year
2010
Tongue
English
Weight
86 KB
Volume
152A
Category
Article
ISSN
1552-4825

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## Abstract We report on a 16‐month‐old male patient with ring chromosome 4 and deletion of Wolf–Hirschhorn syndrome (WHS) region with multiple congenital anomalies including unilateral cleft lip and palate, iris coloboma, microcephaly, midgut malrotation, hypospadias, and double urethral orifices.

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## Abstract ## BACKGROUND Wolf‐Hirschhorn syndrome (WHS) is a well‐known genetic condition characterized by typical facial anomalies, midline defects, skeletal anomalies, prenatal and postnatal growth retardation, hypotonia, mental retardation, and seizures. Affected patients with a microdeletion