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B VARIANT GM2 GANGLIOSIDOSIS [1 record]

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Record 1 2019-04-02

English

Subject field(s)
  • Human Diseases
  • Nervous System
  • Genetics
DEF

… a rare, neurodegenerative disorder in which deficiency of an enzyme (hexosaminidase A) results in excessive accumulation of certain fats (lipids) known as gangliosides in the brain and nerve cells.

French

Domaine(s)
  • Maladies humaines
  • Système nerveux
  • Génétique
DEF

[…] maladie neurodégénérative due à un déficit en hexosaminidase provoquant une accumulation du ganglioside GM2.

Spanish

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