Wolf-Hirschhorn syndrome

(redirected from Wolff-Hirschorn syndrome)

Wolf-Hirschhorn syndrome

 [woolf´hirsh´horn]
a syndrome associated with partial deletion of the short arm of chromosome 4, characterized by an undersized head, increased distance between the eyes, epicanthus, cleft palate, a small receding mandible, low-set ears that are simplified in form, undescended testes, and hypospadias.
Facial view of a 3-year-old child with the Wolf-Hirschhorn syndrome. From Mueller and Young, 2001.
Miller-Keane Encyclopedia and Dictionary of Medicine, Nursing, and Allied Health, Seventh Edition. © 2003 by Saunders, an imprint of Elsevier, Inc. All rights reserved.
An autosomal dominant [MIM 194190] chromosome deletion complex characterised by low birth weight, microcephaly, ‘Greek helmet’ facies—micrognathia, hypertelorism, epicanthus, beaked nose, redundant lateral nasal folds, cleft palate—inguinal hernia, cryptorchism, hypospadias and death before age 3
Segen's Medical Dictionary. © 2012 Farlex, Inc. All rights reserved.

Wolf-Hirschhorn syndrome

(woolf′-hirsh′horn″)
[Kurt Hirschhorn, Austrian-born U.S. geneticist, b. 1926; Ulrich Wolf, Ger. geneticist, b. 1933]
,

WHS

A relatively rare disorder caused by a deletion of the short arm of chromosome 4, which results in the absence of a fibroblast growth factor receptor. Its clinical hallmarks include abnormal facial development, delays in attaining neurological and behavioral milestones, mental retardation, short stature, and heart defects. Affected children often succumb to the disease in the first years of life.
Medical Dictionary, © 2009 Farlex and Partners