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Article

Muenke syndrome.

Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery - 1 May 2004

Sabatino G, Di Rocco F, Zampino G, Tamburrini G, Caldarelli M, Di Rocco C

Abstract excerpt

BACKGROUND: Muenke syndrome is a genetically determined craniosynostosis that involves one or both coronal sutures. In some patients it is associated with skeletal abnormalities such as thimble-like middle phalanges, coned epiphysis, and/or neurological impairment, namely sensorineural hearing loss or mental retardation. In spite of a variable phenotype, Muenke syndrome has been related to a unique mutation on...

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Source

Identifiers

PMID: 14963686
DOI: 10.1007/s00381-003-0906-y

Genes

FGFR3

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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