603896.1

Lebanon

Ataxia; Developmental regression; Leukodystrophy; Metachromatic leukodystrophy variant; Abnormal myelination

Male

Yes

Variant Name	Allele Count	Allele Frequency	Associated Disease	Associated Gene
NM_003907.3:c.407G>A	2		Leukoencephalopathy with Vanishing White Matter