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Canadian Association for Tay-Sachs and Allied Diseases
About the Allied Diseases

Tay-Sachs and the allied diseases are known collectively as lysosomal storage diseases - characterized by a common biochemical defect; the inability of the body's cells to dispose of certain metabolic waste products. These waste products gradually accumulate in the cells of affected children, causing a variety of debilitating symptoms.

CATSAD has also worked with families that have children affected with conditions other than those listed below, particularly mitocondrial disorders.

Lipidoses:


Mucopolysaccharide Disorders: A handbook on MPS disorders is available on line from The Canadian Society for Mucopolysaccharide & Related Diseases
  • Hurler Syndrome (MPS IH)
  • Scheie Syndrome (MPS IS)
  • Hurler-Scheie (MP IH/S)
  • Hunter Syndrom (MPS II)
  • Sanfilippo A (MPS IIIA)
  • Sanfilippo B (MPS IIIB)
  • Sanfilippo C (MPS IIIC)
  • Sanfilippo D (MPS IIID)
  • Morquio A (MPS IVA)
  • Morquio B (MPS IVB)
  • Maroteaux-Lamy (MPS VI)
  • Sly (MPS VII)
Glycoprotein Disorders:
  • Mannosidosis
  • Fucosidosis
  • Aspartylglucosaminuria
  • Sialidosis (Mucolipidosis I)
  • Galactosiaidosis
  • Schindler Disease
Other Lysosomal Storage Disorders:
  • Batten Disease
  • Infantile Neuronal Ceroid Liposuscinosis
  • Pompe Disease
  • Mucolipisosis III
  • Mucolipisosis IV
  • Cystinosis
  • Salla Disease
  • Infantile Sialic Acid Storage Disease
  • Saposin Deficiencies
Non-Lysosomal Diseases:
  • Abetalipoproteinemia
  • X-Linked Adrenoleukodystrophy
  • Refsum Disease
  • Canavan Disease
  • Cerebrotendinous Xanthromatosis Sterol-27-Hydroxylase
  • Pelizaeus Merzbacher Disease
  • Tangier Disease

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updated December 11, 2004