Ophthalmologic manifestations of Waardenburg syndrome

Author:

Astakhov Yu. S.,Tultseva S. N.,Lisochkina A. B.,Takhtaev Yu. V.,Astakhov S. Yu.,Shakhnazarova A. A.

Publisher

Media Sphere Publishing Group

Subject

Ophthalmology

Reference17 articles.

1. Waardenburg PJ. A new syndrome combining developmental anomalies of the eyelids, eyebrows and nose root with pigmentary defects of the iris and head hair and with congenital deafness. Am J Hum Genet. 1951;3(3):195-253.

2. Milunsky JM. Waardenburg Syndrome Type I. 2001 Jul 30 [Updated 2017 May 4]. In: Adam MP, Ardinger HH, Pagon RA, et al, editors. GeneReviews [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2019. Available from: https://www.ncbi.nlm.nih.gov/books/NBK1531/

3. Waardenburg's syndrome.

4. Historical background and evidence for dominant inheritance of the Klein-Waardenburg syndrome (type III)

5. White forelock, pigmentary disorder of irides, and long segment Hirschsprung disease: Possible variant of Waardenburg syndrome

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