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Article

A large Turkish kindred with syndactyly type II (synpolydactyly). 2. Homozygous phenotype?

Journal of medical genetics - 1 Jun 1995

Akarsu A N, Akhan O, Sayli B S, Sayli U, Baskaya G, Sarfarazi M

Abstract excerpt

Syndactyly type II (synpolydactyly (SPD)) is an autosomal dominant condition with typical abnormalities of the distal parts of both upper and lower limbs. We report here a previously undescribed phenotypic feature of people with severe hand and foot deformities who were born to two affected parents. This is the first example of SPD subjects manifesting a very distinctive phenotype, suggesting that they must be...

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Identifiers

PMID: 7666394
DOI: 10.1136/jmg.32.6.435
PMCID: PMC1050482

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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.

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