NARP Neurogenic Ataxia Retinitis Pigmentosa
This genetic test detects mitochondrial DNA mutations associated with NARP syndrome. The condition presents with neuropathy, ataxia, and visual impairment. Molecular confirmation enables accurate diagnosis, prognosis estimation, and genetic counseling for affected individuals and families.
NARP Neurogenic Ataxia Retinitis Pigmentosa
NARP Neurogenic Ataxia Retinitis Pigmentosa
