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Teebi hypertelorism syndrome (brachycephalofrontonasal dysplasia) in a U.S. family.

Authors
  • Stratton, R F
Type
Published Article
Journal
American journal of medical genetics
Publication Date
Apr 01, 1991
Volume
39
Issue
1
Pages
78–80
Identifiers
PMID: 1867268
Source
Medline
License
Unknown

Abstract

Teebi (Am J Med Genet 28:581-591, 1987) described a pattern of anomalies in an Arab kindred involving 16 individuals in 4 generations. Although some findings were similar to those in craniofrontonasal dysplasia, absence of craniosynostosis, normal to slightly broad nasal tip, normal nails, and male to male transmission distinguished this as a separate entity. This paper describes a U.S. family with similar findings, involving 6 individuals (2 male and 4 female) in 4 generations, with male to male transmission.

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