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Skeletal anomalies and deformities in patients with deletions of 22q11.

Authors :
Ming JE
McDonald-McGinn DM
Megerian TE
Driscoll DA
Elias ER
Russell BM
Irons M
Emanuel BS
Markowitz RI
Zackai EH
Source :
American journal of medical genetics [Am J Med Genet] 1997 Oct 17; Vol. 72 (2), pp. 210-5.
Publication Year :
1997

Abstract

Skeletal anomalies in patients with a 22q11.2 deletion are reported infrequently. We report the skeletal findings in 108 patients with a 22q11.2 deletion, of whom 37 (36%) had a skeletal anomaly. Twenty-two patients (20%) had anomalies of the limbs, 7 of the upper limb, including preaxial or postaxial polydactyly. An anomaly of the lower limb was found in 16 patients, including postaxial polydactyly, clubfoot, severely overfolded toes, and 2-3 toe cutaneous syndactyly. Chest films of 63 patients were examined; 30% of them had abnormal findings, most commonly supernumerary ribs (17%) or a "butterfly" vertebral body (11%). Hypoplastic vertebrae, hemivertebrae, and vertebral coronal clefts were also noted. Thus, skeletal anomalies are not uncommon in patients with a 22q11.2 deletion and may occur more frequently than recognized previously.

Details

Language :
English
ISSN :
0148-7299
Volume :
72
Issue :
2
Database :
MEDLINE
Journal :
American journal of medical genetics
Publication Type :
Academic Journal
Accession number :
9382145
Full Text :
https://doi.org/10.1002/(sici)1096-8628(19971017)72:2<210::aid-ajmg16>3.0.co;2-q