|1.||Neuroaxonal Dystrophies (Neuroaxonal Dystrophy, Late Infantile)
08/01/1991 - "Known causes of the cutaneous manifestation were eliminated by enzyme analyses, and further characterization of the accumulated urinary O-linked sialopeptides revealed identity to those excreted by patients with an infantile neuroaxonal dystrophy due to lysosomal alpha-N-acetylgalactosaminidase deficiency. "
06/29/1989 - "Neuroaxonal dystrophy due to lysosomal alpha-N-acetylgalactosaminidase deficiency."
|2.||Metabolic Diseases (Metabolic Disease)
|3.||Fabry Disease (Fabry's Disease)