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Dictionary » Craniosynostosis herrmann opitz type
 

Craniosynostosis herrmann opitz type

Introduction: Craniosynostosis herrmann opitz type

Description of Craniosynostosis herrmann opitz type

Craniosynostosis herrmann opitz type (medical condition): A rare condition characterized mainly by premature fusion of skull bones,...more »

See also:

Craniosynostosis -- brachysyndactyly of hands and absence of toes:
  »Introduction: Craniosynostosis -- brachysyndactyly of hands and absence of toes
  »Symptoms of Craniosynostosis -- brachysyndactyly of hands and absence of toes

Craniosynostosis herrmann opitz type: Related Topics

These medical condition or symptom topics may be relevant to medical information for Craniosynostosis herrmann opitz type:

Craniosynostosis herrmann opitz type: Rare Disease

Ophanet

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

Source - Orphanet

Craniosynostosis herrmann opitz type as a Disease

Craniosynostosis herrmann opitz type: Another name for Craniosynostosis -- brachysyndactyly of hands and absence of toes (or close medical condition association).
  »Introduction: Craniosynostosis -- brachysyndactyly of hands and absence of toes
  »Symptoms of Craniosynostosis -- brachysyndactyly of hands and absence of toes

Craniosynostosis herrmann opitz type: Related Diseases

Craniosynostosis herrmann opitz type: Craniosynostosis herrmann opitz type is listed as a type of (or associated with) the following medical conditions in our database:

Symptoms of Craniosynostosis herrmann opitz type (Craniosynostosis -- brachysyndactyly of hands and absence of toes)

Some of the symptoms of Craniosynostosis herrmann opitz type incude:

Interesting Medical Articles:

Medical dictionaries:

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