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Article

Audiologic Phenotype and Progression in Pediatric STRC-Related Autosomal Recessive Hearing Loss.

The Laryngoscope - 1 Dec 2021

Simi Andrea, Perry Julia, Schindler Emma, Oza Andrea, Luo Minjie, Hartman Tiffiney, Krantz Ian D, Germiller John A, Kawai Kosuke, Kenna Margaret

Abstract excerpt

OBJECTIVES: Sensorineural hearing loss (SNHL) is a common sensory deficit affecting pediatric populations. The majority of pediatric SNHL is genetic in etiology, with over 123 identified nonsyndromic causative genes. One such gene is STRC, which has been identified as the second most frequent autosomal recessive nonsyndromic gene associated with SNHL in multiple populations. The objective of this study was to...

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Source

Identifiers

PMID: 34111299
DOI: 10.1002/lary.29680

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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