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

Short stature, brachydactyly, and Peters' anomaly (Peters'-plus syndrome): confirmation of autosomal recessive inheritance.

Journal of medical genetics - 1 Apr 1991

de Almeida J C, Reis D F, Llerena Júnior J, Barbosa Neto J, Pontes R L, Middleton S, Telles L F

Abstract excerpt

Two sibs with a phenotype characterised by short stature, brachydactyly, and ocular anomalies (Peters' anomaly) are reported (Peters'-plus syndrome). The consanguinity is in agreement with the proposed autosomal recessive inheritance.

Read the complete abstract on PubMed

Topics

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

Share to Child, Preschool
Share to Consanguinity
Share to Cornea

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

Share to Genes, Recessive

Share to Growth Disorders

Share to Infant

Share to Phenotype

Share to Syndrome

Source

Open in PubMed Open full text

Identifiers

PMID: 1856836
DOI: 10.1136/jmg.28.4.277
PMCID: PMC1016833

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 · 8 closest

Short stature, brachydactyly, and Peters' anomaly (Peters'-plus syndrome): confirmation of autosomal recessive inheritance.PMID 1856836Read ↗

Severe short stature, hyperphalangy of the index fingers, mental retardation and facial dysmorphism.Semantic proximity Read ↗

Peters plus syndrome.Semantic proximity Read ↗

Short stature, Robin sequence, cleft mandible, pre/postaxial hand anomalies, and clubfoot: A new autosomal recessive syndromeSemantic proximity Read ↗

Miller syndrome (postaxial acrofacial dysostosis): further evidence for autosomal recessive inheritance and expansion of the phenotype.Semantic proximity Read ↗

Prenatal Diagnosis of Peters-Plus Syndrome: A Case ReportSemantic proximity Read ↗

Hydrocephalus, agenesis of the corpus callosum, and cleft lip/palate represent frequent associations in fetuses with Peters' plus syndrome and B3GALTL mutations. Fetal PPS phenotypes, expanded by Dandy Walker cyst and encephalocele.Semantic proximity Read ↗

How many entities exist for the spectrum of disorders associated with brachydactyly, syndactyly, short stature, microcephaly, and intellectual disability?Semantic proximity Read ↗

A distinctive autosomal recessive syndrome of severe disproportionate short stature with short long bones, brachydactyly, and hypotrichosis in two consanguineous Arab families.Semantic proximity Read ↗

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