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P144 Absence of seizures in a case of Wolf Hirschhorn syndrome with LETM1 deletion

✍ Scribed by C. Galasso; A. Lo-Castro; N. El-Malhany; L. Di Carlo; C. Cerminara; M. Zollino; P. Curatolo


Book ID
114360012
Publisher
Elsevier Science
Year
2009
Tongue
English
Weight
101 KB
Volume
13
Category
Article
ISSN
1090-3798

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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