GTR Home > Conditions/Phenotypes > Ulnar-mammary syndrome

Summary

The ulnar-mammary syndrome is an autosomal dominant disorder characterized by posterior limb deficiencies or duplications, apocrine/mammary gland hypoplasia and/or dysfunction, abnormal dentition, delayed puberty in males, and genital anomalies (Bamshad et al., 1996). [from OMIM]

Genes See tests for all associated and related genes

  • Also known as: TBX3-ISO, UMS, XHL, TBX3
    Summary: T-box transcription factor 3

Clinical features

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