Difference between revisions of "Marfan Syndrome"

From Anthony Nolan Medical Guidelines
Jump to navigation Jump to search
m (Protected "Marfan Syndrome" (‎[edit=sysop] (indefinite) ‎[move=sysop] (indefinite)))
 
(No difference)

Latest revision as of 12:57, 19 June 2012

Acceptability at Recruitment

QUALIFIED

Acceptability at CT / Work-Up

QUALIFIED

Individual at Risk

Donor

Explanation of Condition

Inherited connective tissue disorder. Individuals are often very tall with long limbs and fingers (arachnodactyly). There is a high incidence of congenital cardiac disease.

See also Marfan Syndrome

Guidance

Unacceptable if cardiac involvement. Otherwise discuss with medical officer.

Pseudonyms or Related Conditions

Version

Version 1, Edition 1

Date of Last Update

15th June 2012