Identification of Waardenburg Syndrome and the Management of Hearing Loss and Associated Sequelae: A Review for the Pediatric Nurse Practitioner

Author:

Ringer Jonathan

Publisher

Elsevier BV

Subject

Pediatrics, Perinatology, and Child Health

Reference33 articles.

1. Year 2000 position statement: Principles and guidelines for early hearing detection and intervention,2000

2. Hirschsprung disease, associated syndromes, and genetics: A review;Amiel;Journal of Medical Genetics,2001

3. Cochlear implantation outcomes in children with Waardenburg syndrome;Amirsalari;European Archives of Oto-Rhino-Laryngology,2011

4. Deletions at the SOX10 gene locus cause Waardenburg syndrome types 2 and 4;Bondurand;American Journal of Human Genetics,2007

5. Early childhood: 1–4 years,2019

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1. Comprehensive Approach for the Genetic Diagnosis of Patients with Waardenburg Syndrome;Journal of Personalized Medicine;2024-08-27

2. Deciphering potential causative factors for undiagnosed Waardenburg syndrome through multi-data integration;Orphanet Journal of Rare Diseases;2024-06-06

3. Developmental Anomalies of the Cornea and Iris in Neonates;Principles of Neonatology;2024

4. A Rare Case Report: Waardenburg Syndrome;Proceedings of the 3rd International Conference on Cardiovascular Diseases (ICCvD 2021);2022-12-18

5. A novel SOX10 nonsense mutation in a patient with Kallmann syndrome and Waardenburg syndrome;Endocrinology, Diabetes & Metabolism Case Reports;2021-04-01

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