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Article

The phenotypic spectrum of the 10p deletion syndrome versus the classical DiGeorge syndrome.

Genetic counseling (Geneva, Switzerland) - 1 Jan 1999

Van Esch H, Groenen P, Fryns J P, Van de Ven W, Devriendt K

Abstract excerpt

We reviewed 36 patients with a deletion of the short arm of chromosome 10 and a partial DiGeorge syndrome. We compared the phenotypes observed in these del(10p) patients with the classical DiGeorge phenotype associated with del(22q11), pointing out both similarities and differences. Some features, such as sensorineural hearing loss, seem to be highly associated with a deletion of 10p but are absent in the...

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Share to Abnormalities, Multiple
Share to Chromosome Deletion

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Chromosomes, Human, Pair 10

Share to Chromosomes, Human, Pair 22

Share to Diagnosis, Differential

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Source

Identifiers

PMID: 10191430

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.

Related research

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Research trail→

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The phenotypic spectrum of the 10p deletion syndrome versus the classical DiGeorge syndrome.PMID 10191430Read ↗

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