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

Phenotypic differerencss in African Americans with Prader-Willi syndrome.

Genetics in medicine : official journal of the American College of Medical Genetics - 1 Jan 2000

Hudgins L, Geer J S, Cassidy S B

Abstract excerpt

We report on 10 African Americans with Prader-Willi syndrome whose features differ from those of white patients with this condition. Growth is less affected, hand and foot lengths usually are normal, and the facies are atypical; this may lead to underdiagnosis in this population. We encourage clinicians to recognize these phenotypic differences so that diagnosis is not overlooked.

Read the complete abstract on PubMed

Topics

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

Share to Adolescent
Share to Black or African American
Share to Child

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

Share to Child Development

Share to Child, Preschool

Share to Facies

Share to Infant

Share to Prader-Willi Syndrome

Source

Identifiers

PMID: 11261430
DOI: 10.1097/00125817-199811000-00010

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

Phenotypic differerencss in African Americans with Prader-Willi syndrome.PMID 11261430Read ↗

Neurobehavioral phenotype in Prader-Willi syndrome.Semantic proximity Read ↗

Tall stature. An atypical phenotype in Prader-Willi syndrome.Semantic proximity Read ↗

Behavioral phenotypes in genetic syndromes: genetic clues to human behavior.Semantic proximity Read ↗

Change in prevalence of congenital defects in children with Prader-Willi syndrome.Semantic proximity Read ↗

Prader-Willi syndrome phenotype in X chromosome anomalies: evidence for a distinct syndrome.Semantic proximity Read ↗

Expressive and receptive language in Prader–Willi syndrome: Report on genetic subtype differencesSemantic proximity Read ↗

Prader-Willi syndromeSemantic proximity Read ↗

Next Steps in Prader-Willi Syndrome Research: On the Relationship between Genotype and Phenotype.Semantic proximity Read ↗

Relationship between clinical and genetic diagnosis of Prader-Willi syndrome.Semantic proximity Read ↗

Concurrence of fragile X syndrome and 47, XYY in an individual with a Prader-Willi-like phenotype.Semantic proximity Read ↗

Waardenburg's syndrome: variations in expressivity.Semantic proximity Read ↗

Patterns of inheritance in familial prune belly syndromeSemantic proximity Read ↗

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