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Journal of Medical Genetics logoLink to Journal of Medical Genetics
. 1988 May;25(5):313–321. doi: 10.1136/jmg.25.5.313

Sorsby syndrome: a report on further generations of the original family.

E M Thompson 1, M Baraitser 1
PMCID: PMC1050457  PMID: 3385739

Abstract

Sorsby syndrome is a dominantly inherited combination of bilateral macular colobomas and apical dystrophy of the hands and feet (brachydactyly type B). We report on a further three affected members of the family originally described by Sorsby. Two of these have a single kidney, two have hearing loss, and one has a uterine anomaly.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

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