Preparing service availability
Loading related services
Lahalak Medical PlatformDifferentiate Care
Spinocerebellar Ataxia (SCA) Genetic Test
Advanced molecular analysis to detect mutations causing spinocerebellar ataxia, aiding in accurate diagnosis and understanding inheritance patterns for family health planning.
Molecular genetic analysis to detect abnormal repeats of trinucleotide sequences (often CAG repeats) in specific genes responsible for the most common forms of spinocerebellar ataxia (SCA), types 1, 2, 3 (Machado-Joseph disease), 6, 7, and 17. The number of repeats is determined, as an excess of the normal number is associated with disease occurrence and can be related to age of onset and symptom severity.
Short answers to the FAQs published with this service.
Use Labeeb smart tools to understand reports related to (Medical Laboratories), or search the platform directory directly.
We can help request the service and prepare your inquiry, or you can ask Labeeb to guide you to the most suitable category or service.
Each provider has one service price, then you choose from its available branches.
Related services
