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Multiple Endocrine Neoplasia Type I

Inheritance patterns and prenatal diagnosis

Inheritance patterns
MEN I is inherited as an autosomal dominant trait. Changes in a gene on chromosome 11 (known as MEN I) are associated with the clinical features.

Prenatal diagnosis
This may be possible. Genetic counselling is advised for all individuals and families prior to genetic testing together with further specialist information and support.

View What are the causes? What are the causes?  |  Is there support? View Is there support?

Medical text written September 2003 by Contact a Family. Approved September 2003 by Professor R V Thakker. Last updated January 2006 by Professor R V Thakkar, Head of the Molecular Endocrinology Group, John Radcliffe Hospital, Oxford, UK.

 

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