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Article

Abnormal auditory pathways in PHOX2B mutation positive congenital central hypoventilation syndrome.

BMC neurology - 22 Mar 2015

Trang Ha, Masri Zada Tarif, Heraut Fawzia

Abstract excerpt

BACKGROUND: Congenital central hypoventilation syndrome (CCHS) is a rare disease characterized by severe central hypoventilation due to abnormal autonomic control of breathing. The PHOX2B gene, mutations of which define the disease, is expressed in a group of nuclei located in brainstem areas. Pathways controlling breathing and auditory pathways traverse very similar anatomic structures. In the present study, we...

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Identifiers

PMID: 25886294
DOI: 10.1186/s12883-015-0299-z
PMCID: PMC4391482

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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