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Article

Temporal Bone Histopathology in NOG-Symphalangism Spectrum Disorder.

Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology - 1 Dec 2015

Quesnel Alicia M, Nadol Joseph B, Nielsen G Petur, Curtin Hugh D, Lesperance Marci M

Abstract excerpt

OBJECTIVE: To describe the human temporal bone histopathology in NOG-related symphalangism spectrum disorder, a spectrum of congenital stape fixation syndromes caused by mutations in the NOG gene. To discuss implications for clinical management. PATIENT: A patient with a mutation in the NOG gene. INTERVENTION(S): Removal of temporal bones, postmortem temporal bone computed tomography, histologic processing, and...

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Source

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Identifiers

PMID: 26474326
DOI: 10.1097/MAO.0000000000000861
PMCID: PMC4659774

Genes

NOG

Provenance

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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