FCMD

(redirected from Form of Congenital Muscular Dystrophy)
AcronymDefinition
FCMDFamily and Community Medicine (University of Kansas; Wichita, KS)
FCMDFukuyama Congenital Muscular Dystrophy
FCMDForm of Congenital Muscular Dystrophy (genetics)
FCMDVouka Sidetra (airport code; Congo)
References in periodicals archive ?
A new form of congenital muscular dystrophy with joint hyperlaxity maps to 3p23-21.
Mutations in INPP5K cause a form of congenital muscular dystrophy overlapping marinesco-SjAaAaAeA gren syndrome and dystroglycanopathy.
Mutations in the fukutin-related protein gene (FKRP) cause a form of congenital muscular dystrophy with secondary laminin alpha2 deficiency and abnormal glycosylation of alpha-dystroglycan.
Mutations in the human LARGE gene cause MDC1D, a novel form of congenital muscular dystrophy with severe mental retardation and abnormal glycosylation of alpha-dystroglycan.
Assignment of a form of congenital muscular dystrophy with secondary merosin deficiency to chromosome 1q42.
The patent granted in Canada covers use of omigapil for the treatment or prevention of muscular dystrophy especially congenital muscular dystrophies resulting from laminin-alpha-2 deficiency as in the MDC1A form of congenital muscular dystrophy.