Marfan syndrome. Report of a patient

Marfan syndrome. Report of a patient

Blog Article

Marfan syndrome is a congenital hereditary disease (sporadic in 15-30% of cases) of connective tissue, dominant autosomal with complete penetrance, with prevalence estimated at one per 5 000 people and Protein Bars incidence of one per 10 000 births without racial or sex predominance.A patient with sporadic Marfan syndrome was diagnosed after being Swim Tops benefited with a renal transplantation.Review of the clinical manifestations syndrome of Marfan is done and criteria for diagnosis.