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Article

Malformation of cortical and vascular development in one family with parietal foramina determined by an ALX4 homeobox gene mutation.

AJNR. American journal of neuroradiology - 1 Jan 2000

Valente Marcelo, Valente Kette D, Sugayama Sofia S M, Kim Chong Ae

Abstract excerpt

Vascular and cortical anomalies have been found in a family with parietal foramina type 2 (PFM2), which is determined by the ALX4 gene. It is believed that ALX4 has a bone-restricted expression. We report a case of PFM with age-related size variation in a 4-year-old boy, as well as in his mother,...

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Share to Abnormalities, Multiple
Share to Cerebral Cortex
Share to Genes, Homeobox

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Ossification, Heterotopic

Share to Prosencephalon

Share to Tomography, X-Ray Computed

Source

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Identifiers

PMID: 15569759
PMCID: PMC8148717

Genes

ALX4

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 Sept 2026. Prepared record publication-15569759-2026-09-01.1. Manifest publication-graph-cohort-2026-09-01.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 1 Sept 2026.

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