Atypical presentation of Waardenburg's syndrome type II

Otolaryngology - Head and Neck Surgery

Volumn 120, Issue 5, 1999, Pages 749-

  Knox, Glenn ^a,b   McPherson, Anastasia ^a   Lopes, Anne Marie ^a  

^a HOSPITAL OF THE UNIVERSITY OF PENNSYLVANIA   (United States)

^b NONE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; CASE REPORT; CLINICAL FEATURE; CRANIOFACIAL MALFORMATION; EYE COLOR; EYELID; HAIR COLOR; HETEROTOPIA; HUMAN; MALE; PENETRANCE; PERCEPTION DEAFNESS; TINNITUS; WAARDENBURG SYNDROME;

EID: 13044258877     PISSN: 01945998     EISSN: None     Source Type: Journal    
DOI: 10.1053/hn.1999.v120.a85712     Document Type: Article

References (4)

1. Tsafrir JS. Klein-Waardenburg syndrome. London: MacMillan; 1974. p. 22-5.
2. Waardenburg PJ. A new syndrome combining developmental anomalies of the eyelids, eyebrows and nose root. Am J Hum Genet 1951;3:195-253.
3. Reynolds JE, Marazita ME, Myer JM, et al. Major locus and polygenic contributions to variability of dystopia canthorum in Waardenburg syndrome. Am J Med Genet. In press 1994.
4. Liu XZ, Newton VE, Read AP. Waardenburg syndrome type II: phenotypic findings and diagnostic criteria. Am J Med Genet 55:95-100.