Orocraniodigital syndrome

Introduction: Orocraniodigital syndrome

Description of Orocraniodigital syndrome

Orocraniodigital syndrome (medical condition): A rare hereditary disorder characterized by a growth hormone deficiency as well as mouth and limb abnormalities.

See also:

Juberg-Hayward syndrome:
  »Introduction: Juberg-Hayward syndrome
  »Symptoms of Juberg-Hayward syndrome

Orocraniodigital syndrome: Rare Disease

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

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

Ophanet

Ophanet, a consortium of European partners, currently defines a condition rare when if affects 1 person per 2,000. They list Orocraniodigital syndrome as a "rare disease".

Source - Orphanet

Orocraniodigital syndrome as a Disease

Orocraniodigital syndrome: Another name for Juberg-Hayward syndrome (or close medical condition association).
  »Introduction: Juberg-Hayward syndrome
  »Symptoms of Juberg-Hayward syndrome

Symptoms of Orocraniodigital syndrome (Juberg-Hayward syndrome)

Some of the symptoms of Orocraniodigital syndrome incude:

• Cleft lip
• Cleft palate
• Small head
• Underdeveloped thumb
• Absence of thumbs

See full list of 11 symptoms of Orocraniodigital syndrome (Juberg-Hayward syndrome)

Terms associated with Orocraniodigital syndrome:

Terms Similar to Orocraniodigital syndrome:

• Juberg Hayward syndrome
• Cleft lip/palate with abnormal thumbs and microcephaly

Source - NIH

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