A case of Waardenburg syndrome type I with congenital sensorineural hearing loss-Reference-Cited by-同舟云学术

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A case of Waardenburg syndrome type I with congenital sensorineural hearing loss

Published:2023-06-09 Issue:1 Volume:8 Page:83-86
ISSN:2377-2484
Container-title:Acta Oto-Laryngologica Case Reports
language:en
Short-container-title:Acta Oto-Laryngologica Case Reports

Author:

Le-Tran Quang Minh¹²,Nguyen Duc Phu³,Huynh Quang Huy⁴^ORCID

Affiliation:

1. Ear Nose Throat Hospital, Ho Chi Minh City, Vietnam

2. Otorhinolaryngology Department, Pham Ngoc Thach University of Medicine, Ho Chi Minh City, Vietnam

3. Otology Department, Ear Nose Throat Hospital, Ho Chi Minh city, Vietnam

4. Radiology Department, Pham Ngoc Thach University, Ho Chi Minh city, Vietnam

Publisher

Informa UK Limited

Subject

Modeling and Simulation

Link

https://www.tandfonline.com/doi/pdf/10.1080/23772484.2023.2221090

Reference11 articles.

1. 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;Waardenburg PJ.;Am J Hum Genet,1951

2. Waardenburg Syndrome Type 1

3. Ahmed Jan N, Mui RK, Masood S. Waardenburg syndrome, in StatPearls. 2022. Treasure Island, FL: StatPearls.

4. Hearing loss in Waardenburg syndrome: a systematic review

5. Waardenburg syndrome (WS) type I is caused by defects at multiple loci, one of which is near ALPP on chromosome 2: first report of the WS consortium;Farrer LA;Am J Hum Genet,1992

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