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Learn About Waardenburg Syndrome Type 1

What is the definition of Waardenburg Syndrome Type 1?
Waardenburg syndrome type 1 is a genetic condition characterized by eyes that appear widely spaced, congenital hearing loss, and patchy pigment disturbances of the iris, hair and skin. Genetic changes in the PAX3 gene cause the symptoms observed in this condition. Waardenburg syndrome type 1 is inherited in an autosomal dominant manner.
What are the alternative names for Waardenburg Syndrome Type 1?
  • Waardenburg syndrome type 1
  • WS1
  • Waardenburg's syndrome type 1
Who are the top Waardenburg Syndrome Type 1 Local Doctors?
Elite in Waardenburg Syndrome Type 1
Elite in Waardenburg Syndrome Type 1
UMR_S955, Université Paris Est, 
Creteil, FR 

Veronique Pingault practices in Creteil, France. Ms. Pingault is rated as an Elite expert by MediFind in the treatment of Waardenburg Syndrome Type 1. Her top areas of expertise are Waardenburg Syndrome Type 1, Waardenburg Syndrome, Waardenburg Syndrome Type 2, and Deafness Hypogonadism Syndrome.

Elite in Waardenburg Syndrome Type 1
Elite in Waardenburg Syndrome Type 1
Paris, FR 

Sandrine Marlin practices in Paris, France. Ms. Marlin is rated as an Elite expert by MediFind in the treatment of Waardenburg Syndrome Type 1. Her top areas of expertise are Hearing Loss, Acrofrontofacionasal Dysostosis Syndrome, Treacher Collins Syndrome, Acrofacial Dysostosis Rodriguez Type, and Osteotomy.

 
 
 
 
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Paul T. Baird
Advanced in Waardenburg Syndrome Type 1
Internal Medicine
Advanced in Waardenburg Syndrome Type 1
Internal Medicine

Emory Saint Joseph's Hospital Campus

5673 Peachtree Dunwoody Road, Fl5, 
Atlanta, GA 
Experience:
30+ years
Languages Spoken:
English
Offers Telehealth

Paul Baird is a primary care provider, practicing in Internal Medicine in Atlanta, Georgia. Dr. Baird has been practicing medicine for over 30 years and is rated as an Advanced provider by MediFind in the treatment of Waardenburg Syndrome Type 1. His top areas of expertise are Waardenburg Syndrome Type 1, Waardenburg Syndrome, Monoamine Oxidase A Deficiency, and Waardenburg Syndrome Type 2.

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Published Date: May 02, 2022
Published By: Genetic and Rare Diseases Informnation Center