Short stature, brachydactyly, and Peters' anomaly (Peters'-plus syndrome): confirmation of autosomal recessive inheritance.
case_report · Level V
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- Record sourced from PubMed, PMID 1856836.
- Also identified by PMC identifier 1016833.
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Abstract
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.
Medical subject headings
- Cornea
- Genes, Recessive
- Growth Disorders