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Marfan Syndrome Type II

MedGen UID:
437417
Concept ID:
C2698016
Disease or Syndrome
 

Definition

Marfan syndrome caused by mutations in the TGFBR2 gene. [from NCI]

Term Hierarchy

CClinical test,  RResearch test,  OOMIM,  GGeneReviews,  VClinVar  
  • CROGVMarfan Syndrome Type II

Recent clinical studies

Diagnosis

Zangwill SD, Brown MD, Bryke CR, Cava JR, Segura AD
Congenit Heart Dis 2006 Sep;1(5):229-32. doi: 10.1111/j.1747-0803.2006.00040.x. PMID: 18377530

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