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Article

The otolaryngologic manifestations of Sotos syndrome.

International journal of pediatric otorhinolaryngology - 1 Nov 2013

Gaudreau Philip, Zizak Vincent, Gallagher Thomas Q

Abstract excerpt

OBJECTIVE: Soto's syndrome is a genetic disorder caused by mutations in the NSD1 gene. It is characterized by excessive growth in early life. It features craniofacial abnormalities, developmental delay, hypotonia and advanced bone age. A review of the current literature reveals only chronic otitis media and conductive hearing loss as otolaryngologic manifestations of Soto's syndrome. Our objective was to...

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Source

Identifiers

PMID: 24060089
DOI: 10.1016/j.ijporl.2013.08.029

Genes

NSD1

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.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

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The otolaryngologic manifestations of Sotos syndrome.PMID 24060089Read ↗

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A clinical study of Sotos syndrome patients with review of the literature.Semantic proximity Read ↗

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A novel nonsense variant in NSD1 gene in a female child with Sotos syndrome: A case report and literature review.Semantic proximity Read ↗

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