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C1 Esterase Inhibitor Deficiency

Inheritance patterns and prenatal diagnosis

Inheritance patterns
C1 esterase inhibitor deficiency is autosomal dominant. Non-hereditary C1 esterase inhibitor deficiency is very rare, and usually starts in middle age.

Prenatal diagnosis
Not routinely available.

View How is it treated? How is it treated?  |  Is there support? View Is there support?

Medical text written September 2001 by Dr H Longhurst. Last updated September 2005 by Dr H Longhurst, Consultant Immunologist, St Bartholomew's Hospital, London, UK.

 

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