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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.

Topics

Child, Preschool
Consanguinity
Cornea
Female
Genes, Recessive
Growth Disorders
Humans
Infant
Male
Phenotype
Syndrome

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

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

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 29 Aug 2026. Prepared record publication-1856836-2026-08-29.1. Manifest publication-graph-cohort-2026-08-29.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 29 Aug 2026.

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