Teebi hypertelorism syndrome

@article{Koenig2003TeebiHS,
  title={Teebi hypertelorism syndrome},
  author={Rainer Koenig},
  journal={Clinical Dysmorphology},
  year={2003},
  volume={12},
  pages={187–189}
}
  • R. Koenig
  • Published 2003
  • Medicine
  • Clinical Dysmorphology
&NA; Teebi (1987) described an autosomal dominant syndrome with resemblance to craniofrontonasal dysplasia. Here we present a 2 year 5 month old girl with Teebi syndrome showing a prominent forehead, hypertelorism, mild exophthalmos, downslanting palpebral fissures, a depressed nasal bridge, a broad nasal tip, a long philtrum, natal teeth, a thin upper lip, an everted lower lip, a small chin, low‐set ears, preauricular fistulas, a short neck, mild pectus excavatum, an umbilical hernia… Expand
Atrioventricular block and wiry hair in Teebi hypertelorism syndrome
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TLDR
An additional case of Teebi hypertelorism syndrome is reported, with a 6-year-old girl presented with brachycephaly, peculiar facial appearance resembling mild frontonasal "dysplasia", small hands and feet with interdigital webbing, and mild shawl scrotum. Expand
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A 34-month-old boy presented with clinical manifestations of Teebi hypertelorism syndrome including prominent forehead with frontal bossing, hypertelorism, exophthalmos due to shallow orbits, a shortExpand
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TLDR
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TLDR
A large Arab kindred with 16 individuals in 4 generations having an apparently new autosomal dominant syndrome with features of craniofrontonasal dysplasia but with normal or slightly broad nasal tip and without evidence of craniosynostosis or nail abnormalities is described. Expand
New autosomal dominant syndrome resembling craniofrontonasal dysplasia
TLDR
A large Arab kindred with 16 individuals in 4 generations having an apparently new autosomal dominant syndrome with features of Craniofrontonasal dysplasia but with normal or slightly broad nasal tip and without evidence of craniosynostosis or nail abnormalities is described. Expand
Teebi hypertelorism syndrome: report of a third family
We report a mother and daughter who have hypertelorism, mild limb defects, umbilical hernia/omphalocele, natal teeth and minor craniofacial anomalies. These individuals represent the third familyExpand
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