D0060
Duplication SNRPN in Autism
Test Details: Fluorescence in situ hybridization (FISH) is a technique for detecting and locating a specific DNA sequence on a chromosome. Three distinct neurodevelopmental disorders arise primarily from deletions or duplications that occur at the 15q11-q13 locus: Prader-Willi syndrome (PWS), Angelman syndrome (AS) and 15q11-q13 duplication syndrome (Dup15q syndrome). SNRPN gene duplication is associated with neurodevelopmental disabilities. FISH is typically done in conjunction with a karyotype.
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Category
Cytogenetics
Pre-test Information
Clinical history is mandatory.
Report Delivery
6 working days
Gender
All
Organ
Multi-Organ
Duplication SNRPN in Autism
4950
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