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Dictionary » Kjellin syndrome
 

Kjellin syndrome

Introduction: Kjellin syndrome

Description of Kjellin syndrome

Kjellin syndrome (medical condition): A rare syndrome characterized mainly by progressive stiffness and increased...more »

See also:

Spastic paraplegia 15, autosomal recessive:
  »Introduction: Spastic paraplegia 15, autosomal recessive
  »Symptoms of Spastic paraplegia 15, autosomal recessive

Kjellin syndrome: Rare Disease

Office of Rare Diseases (ORD) of the National Institutes of Health (NIH)

Kjellin syndrome is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Kjellin syndrome, or a subtype of Kjellin syndrome, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

Kjellin syndrome as a Disease

Kjellin syndrome: Another name for Spastic paraplegia 15, autosomal recessive (or close medical condition association).
  »Introduction: Spastic paraplegia 15, autosomal recessive
  »Symptoms of Spastic paraplegia 15, autosomal recessive

Kjellin syndrome: Related Diseases

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

Symptoms of Kjellin syndrome (Spastic paraplegia 15, autosomal recessive)

Some of the symptoms of Kjellin syndrome incude:

Terms associated with Kjellin syndrome:

Terms Similar to Kjellin syndrome:

Source - NIH

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