Ulnar-Mammary Syndrome
Analysis ID 44
Analysis location “GENESIS” Centre for Medical Genetics
Diagnosed illness Ulnar-Mammary Syndrome
OMIM #181450
Clinical information Ulnar-Mammary Syndrome – autosomal dominant rare genetic disorder characterized by ulnar oligodactyly, apocrine gland hypoplasia, reduced sweating, as well anal and genitourinary abnormalities.
Type of analysis molecular
Type of biological material 5 ml peripheral blood collected in the EDTA tube
Analyzed genes TBX3
Analysis description Sequencing analysis of the TBX3gene
Analysis indication Symptoms of Ulnar-Mammary Syndrome
Analysis time 3-4 weeks
Refund No
CGM laboratory name Laboratory for diagnostics of the hereditary disorders