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Dictionary » Sphingolipid storage disease
 

Sphingolipid storage disease

Introduction: Sphingolipid storage disease

Description of Sphingolipid storage disease

Sphingolipid storage disease: A group of inherited metabolic disorders characterized by an excessive intra-lysosomal deposition of glycosphingolipids and phosphosphingolipids in the CENTRAL NERVOUS SYSTEM and, to a variable degree, in visceral structures. Clinical features vary with the specific subtype of the disease, but common features include progressive deterioration in psychomotor and visual function. (From Arch Neurol 1998 Aug;55(8):1055-6; Menkes, Textbook of Child Neurology, 5th ed, p89)
Source: Diseases Database

Sphingolipid storage disease: Related Topics

These medical condition or symptom topics may be relevant to medical information for Sphingolipid storage disease:

Terms associated with Sphingolipid storage disease:

Terms Similar to Sphingolipid storage disease:

Source: Diseases Database

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  • Microscopic examination-I
  • Microscopic examination-II
  • Microscopic field
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