Scholz disease

Introduction: Scholz disease

Description of Scholz disease

Scholz disease (medical condition): An infantile form of an inherited biochemical disorder involving a...more »

See also:

Familial infantile metachromatic leukodystrophy -- late infantile:
  »Introduction: Familial infantile metachromatic leukodystrophy -- late infantile
  »Symptoms of Familial infantile metachromatic leukodystrophy -- late infantile

Scholz disease: Related Topics

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

• Scholz
• Scholz disease
• Eponymic
• Term
• Juvenile
• Form
• Metachromatic
• Leukodystrophy

Scholz disease as a Disease

Scholz disease: Another name for Familial infantile metachromatic leukodystrophy -- late infantile (or close medical condition association).
  »Introduction: Familial infantile metachromatic leukodystrophy -- late infantile
  »Symptoms of Familial infantile metachromatic leukodystrophy -- late infantile

Scholz disease: Related Diseases

Scholz disease: Scholz disease is listed as a type of (or associated with) the following medical conditions in our database:

• Infant health conditions
• Nervous system conditions
• Degenerative conditions
• Genetic conditions
• Metabolic conditions
• Congenital conditions - metabolic disorders
• Congenital conditions
• Lipid metabolism conditions

Symptoms of Scholz disease (Familial infantile metachromatic leukodystrophy -- late infantile)

Some of the symptoms of Scholz disease incude:

• Normal initial development
• Irritability - initial symptoms
• Progressive loss of muscle tone
• Progressive weakness
• Progressive loss of reflexes

See full list of 26 symptoms of Scholz disease (Familial infantile metachromatic leukodystrophy -- late infantile)

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Medical dictionaries:

• Medical dictionary,
• Medical Acronymns/Abbreviations

More Medical Dictionary Topics

Proteodermatan sulfate (PDS), defective biosynthesis of

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