Health care resources for this disease expert centres diagnostic tests patient organisations 55 orphan drug s 1. Distrofia miotonica tipo 1 genetic and rare diseases. Distrofia miotonica steinert euniversitate boli rare. Alfredo rosado bartolome a,b y lucia sierra santos a,c. Myotonic dystrophy is a significant cause of idiopatic polyhydramnios. E una malattia muscolare atrofizzante che interessa. The clinical findings, which span a continuum from mild to severe, have been categorized into three somewhat overlapping phenotypes. Early electromyographic signs in congenital myotonic dystrophy. Definizione e una malattia genetica, autosomica dominante caratterizzata da una perdita di forza progressiva. Distrofia miotonica wikipedia, a enciclopedia livre. Myotonic dystrophy type 1 dm1 is a multisystem disorder that affects skeletal and smooth muscle as well as the eye, heart, endocrine system, and central nervous system. E melhor cingirmonos a um so nome distrofia miotonica. Distrofia miotonica di steinert tipo 1 e distrofia. University of minnesota press, kant and the new philosophy of religion.
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