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Dictionary » Congenital radio-ulnar synostosis
 

Congenital radio-ulnar synostosis

Introduction: Congenital radio-ulnar synostosis

Description of Congenital radio-ulnar synostosis

Congenital radio-ulnar synostosis (medical condition): A very rare syndrome characterized by fusion of the forearm bones (radius and...more »

See also:

Radioulnar synostosis type 1:
  »Introduction: Radioulnar synostosis type 1
  »Symptoms of Radioulnar synostosis type 1

Congenital radio-ulnar synostosis: Related Topics

These medical condition or symptom topics may be relevant to medical information for Congenital radio-ulnar synostosis:

Congenital radio-ulnar synostosis: Rare Disease

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

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

Congenital radio-ulnar synostosis as a Disease

Congenital radio-ulnar synostosis: Another name for Radioulnar synostosis type 1 (or close medical condition association).
  »Introduction: Radioulnar synostosis type 1
  »Symptoms of Radioulnar synostosis type 1

Symptoms of Congenital radio-ulnar synostosis (Radioulnar synostosis type 1)

Some of the symptoms of Congenital radio-ulnar synostosis incude:

  • Restricted forearm movement
  • Fused forearm bones
  • Short forearm
  • Impaired hand control

Terms associated with Congenital radio-ulnar synostosis:

Terms Similar to Congenital radio-ulnar synostosis:

Source - NIH

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