Al-Awadi Syndrome
Analysis ID 65
Analysis location “GENESIS” Centre for Medical Genetics
Diagnosed illness Al-Awadi Syndrome
OMIM #276820
Clinical information Al-Awadi syndrome is an allelic disease to Furhmann syndrome, and is caused by mutations in the WNT7A. Symptoms (limb hypoplasia of variable degree) are more severe than those observed in Fuhrmann syndrome.
Type of analysis molecular
Type of biological material 5 ml peripheral blood collected in the EDTA tube
Analyzed genes WNT7A
Analysis description Sequencing analysis of the WNT7A gene.
Analysis indication Symptoms of Al-Awadi Syndrome
Analysis time 3-4 weeks
Refund Yes
CGM laboratory name Laboratory for diagnostics of the hereditary disorders