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Teebi hypertelorism syndrome.
Clin Dysmorphol. 2003 Jul; 12(3):187-9.CD

Abstract

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, clinodactyly of the 5th fingers with mild radial deviation of the distal phalanges of the middle fingers, mild pes adductus, an ectopic kidney, and normal psychomotor development. Her mother and her grandmother had similar features.

Authors+Show Affiliations

Institute of Human Genetics, Johann Wolfgang Goethe University, Frankfurt, Germany. r.koenig@em.uni-frankfurt.de

Pub Type(s)

Case Reports
Journal Article

Language

eng

PubMed ID

14564158

Citation

Koenig, Rainer. "Teebi Hypertelorism Syndrome." Clinical Dysmorphology, vol. 12, no. 3, 2003, pp. 187-9.
Koenig R. Teebi hypertelorism syndrome. Clin Dysmorphol. 2003;12(3):187-9.
Koenig, R. (2003). Teebi hypertelorism syndrome. Clinical Dysmorphology, 12(3), 187-9.
Koenig R. Teebi Hypertelorism Syndrome. Clin Dysmorphol. 2003;12(3):187-9. PubMed PMID: 14564158.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Teebi hypertelorism syndrome. A1 - Koenig,Rainer, PY - 2003/10/18/pubmed PY - 2004/3/17/medline PY - 2003/10/18/entrez SP - 187 EP - 9 JF - Clinical dysmorphology JO - Clin Dysmorphol VL - 12 IS - 3 N2 - 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, clinodactyly of the 5th fingers with mild radial deviation of the distal phalanges of the middle fingers, mild pes adductus, an ectopic kidney, and normal psychomotor development. Her mother and her grandmother had similar features. SN - 0962-8827 UR - https://www.unboundmedicine.com/medline/citation/14564158/Teebi_hypertelorism_syndrome_ L2 - https://doi.org/10.1097/01.mcd.0000077563.66911.c4 DB - PRIME DP - Unbound Medicine ER -