We report on six new families (12 new patients) with the syndrome of microcephaly, facial and hand abnormalities, tracheoesophageal fistula, duodenal atresia, and developmental delay. The most common findings were hand abnormalities, microcephaly, short and/or narrow palpebral fissures, broad nasal
Sandrow syndrome of mirror hands and feet and facial abnormalities
โ Scribed by Kogekar, Nandini ;Teebi, Ahmad S. ;Vockley, Jerry
- Publisher
- John Wiley and Sons
- Year
- 1993
- Tongue
- English
- Weight
- 259 KB
- Volume
- 46
- Category
- Article
- ISSN
- 0148-7299
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โฆ Synopsis
Abstract
In 1970, Sandrow et al. (J Bone Joint Surg 52โA:363โ370) described a syndrome of ulnar and fibular dimelia with facial abnormalities present in 2 generations in a family. We describe a new patient with similar manifestations, establishing this constellation of anomalies as a distinct syndrome. ยฉ 1993 WileyโLiss, Inc.
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