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Article

Syndromic foramina parietalia permagna.

American journal of medical genetics - 6 Aug 1998

Chrzanowska K, Kozlowski K, Kowalska A

Abstract excerpt

We report on a boy with unique somatic and skeletal manifestations. The syndrome consists of branchial and auricular fistulae, abnormal face, and skeletal abnormalities including foramina parietalia permagna.

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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 9714003
DOI: 10.1002/(sici)1096-8628(19980806)78:5<401::aid-ajmg1>3.0.co;2-o

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.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Syndromic foramina parietalia permagna.PMID 9714003Read ↗

Foramina parietalia permagna: the ins and outs.Semantic proximity Read ↗

A novel mutation in the MSX2 gene in a family with foramina parietalia permagna (FPP).Semantic proximity Read ↗

Foramina parietalia permagna: Clinical radiological evaluation of a Spanish family with an undescribed mutation in the ALX4 gene.Semantic proximity Read ↗

A novel mutation in the MSX2 homeobox gene of a family with foramina parietalia permagna, headache and vascular anomaly.Semantic proximity Read ↗

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

Prominent basal emissary foramina in syndromic craniosynostosis: correlation with phenotypic and molecular diagnoses.Semantic proximity Read ↗

Epilepsy in one family with parietal foramina: an incidental finding?Semantic proximity Read ↗

The ALX4 homeobox gene is mutated in patients with ossification defects of the skull (foramina parietalia permagna, OMIM 168500).Semantic proximity Read ↗

[Mother and son with enlarged parietal foramina, persistent fetal vein, and ALX4 mutation].Semantic proximity Read ↗

Identification of mutations in the MSX2 homeobox gene in families affected with foramina parietalia permagna.Semantic proximity Read ↗

Branchiootic syndrome--a clinical case report and review of the literature.Semantic proximity Read ↗

Enlarged parietal foramina.Semantic proximity Read ↗

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