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Article

Molecular Biology of Pediatric Hydrocephalus and Hydrocephalus-related Diseases.

Neurologia medico-chirurgica - 1 Jan 2015

Yamasaki Mami, Kanemura Yonehiro

Abstract excerpt

We are beginning to understand the molecular biology of hydrocephalus and its related diseases. X-linked hydrocephalus (XLH), holoprosencephaly (HPE), Dandy-Walker malformation (DWM), and neural tube defect (NTD) can all be discussed with respect to their available molecular genetics knowledge base and its clinical applications. XLH is single gene disorder caused by mutations in the neural cell adhesion...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

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Identifiers

PMID: 26227058
DOI: 10.2176/nmc.ra.2015-0075
PMCID: PMC4628154

Genes

CELSR1
CELSR2
FOXC1
SHH
SIX3
VANGL1
VANGL2
ZIC1
ZIC2
ZIC4

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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