Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Wolf-Hirschhorn syndrome (WHS) - literature review on the features of the syndrome.

Advances in clinical and experimental medicine : official organ Wroclaw Medical University - 1 Jan 2000

Paradowska-Stolarz Anna M

Abstract excerpt

Wolf-Hirschhorn syndrome (WHS) is a congenital disorder associated with 4 chromosome microdeletion. The patients suffer from various deformities. Among them, mental and growth retardation, even in the fetus, are observed. Most of the characteristics concern facial features. The "Greek warrior helmet appearance" is the most characteristic feature and refers to the facial view with prominent glabella, high arched...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Chromosome Deletion
Share to Chromosomes, Human, Pair 4

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

Share to Diagnosis, Differential

Share to MSX1 Transcription Factor

Share to Predictive Value of Tests

Share to Prenatal Diagnosis

Share to Tooth Abnormalities

Source

Identifiers

PMID: 24979523
DOI: 10.17219/acem/24111

Genes

MSX1

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

Wolf-Hirschhorn syndrome (WHS) - literature review on the features of the syndrome.PMID 24979523Read ↗

Clinical features in adult patient with Wolf-Hirschhorn syndrome.Semantic proximity Read ↗

Prenatal ultrasound findings observed in the Wolf-Hirschhorn syndrome: data from the registry of congenital malformations in Auvergne.Semantic proximity Read ↗

[Wolf-Hirschhorn syndrome. Description of a Spanish cohort of 51 cases and a literature review].Semantic proximity Read ↗

A rare subtelomeric deletion syndrome: Wolf Hirschhorn syndrome.Semantic proximity Read ↗

Wolf-Hirschhorn syndrome: A case series from India.Semantic proximity Read ↗

Wolf-Hirschhorn Syndrome: Clinical and Genetic Study of 7 New Cases, and Mini ReviewSemantic proximity Read ↗

Clinical and genetic characterization of ten Egyptian patients with Wolf-Hirschhorn syndrome and review of literature.Semantic proximity Read ↗

Wolf-Hirschhorn (4p-) syndrome.Semantic proximity Read ↗

Update on the clinical features and natural history of Wolf-Hirschhorn (4p-) syndrome: experience with 87 patients and recommendations for routine health supervision.Semantic proximity Read ↗

Ocular manifestations in Wolf-Hirschhorn syndrome.Semantic proximity Read ↗

From Wolf-Hirschhorn syndrome to NSD2 haploinsufficiency: a shifting paradigm through the description of a new case and a review of the literature.Semantic proximity Read ↗

Prenatal phenotype of Wolf-Hirschhorn syndrome: A case series and literature review.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.