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Article

A unique case of lissencephaly with Crouzon syndrome heterozygous for FGFR2 mutation.

Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery - 1 Jan 2018

Tan Ai Peng, Mankad Kshitij

Abstract excerpt

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Topics

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Share to Brain
Share to Craniofacial Dysostosis
Share to FGFR2 gene
Share to Infant, Newborn

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Lissencephaly

Share to Magnetic Resonance Imaging

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Share to Receptor, Fibroblast Growth Factor, Type 2

Source

Identifiers

PMID: 29067506
DOI: 10.1007/s00381-017-3646-0

Genes

FGFR2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

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A unique case of lissencephaly with Crouzon syndrome heterozygous for FGFR2 mutation.PMID 29067506Read ↗

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