Usher syndrome
Analysis ID 173
Analysis location Collaboration with another facility
Diagnosed illness Usher syndrome
OMIM #276900, #276901, #276902, #276904, #601067, #602083, #602097, #605472, #606943, #611383, #612632, #614504
Clinical information Usher syndrome is a condition characterized by deafness and progressive vision loss (due to retinitis pigmentosa). The degree of symptoms depends on the type of the disease and varies greatly among the affected family members.
Type of analysis Microarray
Type of biological material 5 ml of peripheral blood collected in an ETDA tube; DNA sample
Analyzed genes
Analysis description Analysis consists of 429 mutations in 8 genes studied with use of microarray technology
Analysis indication Symptoms of Usher syndrome
Analysis time Appointed individually
Refund No
CGM laboratory name