z-logo
open-access-imgOpen Access
4p- (Wolf-Hirschhorn) syndrome
Author(s) -
Magill Hl,
Gary D. Shackelford,
McAlister Wh,
Graviss Er
Publication year - 1980
Publication title -
american journal of roentgenology
Language(s) - Uncategorized
Resource type - Journals
SCImago Journal Rank - 1.294
H-Index - 196
eISSN - 1546-3141
pISSN - 0361-803X
DOI - 10.2214/ajr.135.2.283
Subject(s) - medicine , differential diagnosis , pelvis , genetic syndromes , ossification , karyotype , cervical spine , pathology , radiology , pediatrics , anatomy , chromosome , surgery , genetics , biology , gene
The 4p- syndrome results from a structural deficiency in chromosome 4. The clinical and radiologic findings in three patients with the 4p- syndrome are presented. Clinical, genetic, and radiologic findings in other reported cases are summarized. A widened interpubic distance with underdevelopment of the bony pelvis and deficiencies in ossification of the cervical spine are prominent radiologic features in our cases. Taken separately, these findings have limited differential diagnostic possibilities which are briefly discussed. The combination of these findings with characteristic clinical abnormalities is very suggestive of the 4p- syndrome and should prompt karyotyping for confirmation.

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom