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Glossary for Hypotonia related to gray matter disease

Medical terms related to Hypotonia related to gray matter disease or mentioned in this section include:

  • Allan-Herndon-Dudley Syndrome: A very rare inherited disorder characterized primarilty by mental retardation.
  • Alpers Syndrome: A rare syndrome characterized by liver disease, seizures and progressive, episodic psychomotor retardation.
  • GM1 gangliosidosis: A rare biochemical disorder involving a deficiency of an enzyme (beta-galactosidase A) which results in the accumulation of harmful chemicals (GM1 gangliosides) in the central nervous system and other body tissues. Type 1 is a severe infantile form of the disorder and involves a greater degree of accumulation than type II or III.
  • Graying: Gray coloring of the hair
  • Menkes Disease: Genetic disease of copper deficiency.
  • Muscle weakness: Weakness of the muscles or loss of tone
  • Oliver-McFarlane syndrome: A rare genetic condition characterized by mental retardation, dwarfism, retinal pigmentary degeneration and hairy eyelashes and eyebrows.
  • Tay Sachs Disease: A condition which is causes GM2 gangliosidosis

Conditions listing medical symptoms: Hypotonia related to gray matter disease:

The following list of conditions have 'Hypotonia related to gray matter disease' or similar listed as a symptom in our database. This computer-generated list may be inaccurate or incomplete. Always seek prompt professional medical advice about the cause of any symptom.

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