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The Dubowitz syndrome: Further observations

✍ Scribed by Orrison, William W. ;Schnitzler, Eugene R. ;Chun, Raymond W. M. ;Optiz, John M.

Publisher: John Wiley and Sons
Year: 1980
Tongue: English
Weight: 743 KB
Volume: 7
Category: Article
ISSN: 0148-7299
DOI: 10.1002/ajmg.1320070209

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✦ Synopsis

Abstract

An autosomal recessive disorder characterized by intrauterine growth retardation, postnatal retardation, microcephaly, sparse hair, toe syndactyly, and characteristic facial appearance is now recognized as the Dubowitz syndrome. Five addition additional cases of the Dubowitz syndrome are reported, including 2 with documented vascular abnormalities.

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