Multiple pterygium syndrome, autosomal recessive

Introduction: Multiple pterygium syndrome, autosomal recessive

Description of Multiple pterygium syndrome, autosomal recessive

Multiple pterygium syndrome, autosomal recessive (medical condition): A very rare disorder characterized by webbing of various parts of the body, contractures, short stature, fusion of neck vertebrae and facial anomalies.

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Multiple pterygium syndrome, autosomal recessive:
  »Introduction: Multiple pterygium syndrome, autosomal recessive
  »Symptoms of Multiple pterygium syndrome, autosomal recessive

Multiple pterygium syndrome, autosomal recessive: Related Topics

These medical condition or symptom topics may be relevant to medical information for Multiple pterygium syndrome, autosomal recessive:

• Multiple pterygium syndrome
• Pterygium syndrome
• Autosomal recessive
• Pterygium
• Autosomal
• Recessive

Multiple pterygium syndrome, autosomal recessive: Rare Disease

Ophanet

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

Source - Orphanet

Multiple pterygium syndrome, autosomal recessive as a Disease

Multiple pterygium syndrome, autosomal recessive (medical condition): See Multiple pterygium syndrome, autosomal recessive (disease information).
  »Introduction: Multiple pterygium syndrome, autosomal recessive
  »Symptoms of Multiple pterygium syndrome, autosomal recessive

More information on medical condition: Multiple pterygium syndrome, autosomal recessive:

• Information about Multiple pterygium syndrome, autosomal recessive
• Basic Summary for Multiple pterygium syndrome, autosomal recessive
• Symptoms of Multiple pterygium syndrome, autosomal recessive

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