Results for Query ‹ Metachromatic Leukodystrophy Due to Cerebroside Sulfatase Activator Deficiency medication

Laminopathy – Treatment and drug development

Primary immunodeficiency – Treatment

Sanfilippo syndrome – Treatment

Lysosomal storage disease – Treatment

Bare lymphocyte syndrome – Treatment

Primary immunodeficiency – Research

N-Acetylglutamate synthase deficiency – Treatment

Lipid storage disorder – Treatment

X-linked ichthyosis – Treatment

Leukodystrophy – Treatment

Mucopolysaccharidosis – Treatment

Metachromatic leukodystrophy – Treatment

Infantile Refsum disease – Management/prognosis

Hunter syndrome – Treatment | Enzyme replacement

Hunter syndrome – Treatment | Palliative treatment

Morquio syndrome – Treatment

Krabbe disease – Treatment

Metachromatic leukodystrophy – Research | Enzyme replacement therapy (ERT)

X-linked recessive chondrodysplasia punctata – Treatment

Vitamin B12 deficiency – Treatment

Winchester syndrome – Treatment

Alexander disease – Treatment

Barraquer–Simons syndrome – Treatment

Vitamin B12 deficiency – Diagnosis | Effect of folic acid

Leukoencephalopathy with vanishing white matter – Treatment