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Indian Pediatr ; 48(7): 565-7, 2011 Jul.
Article in English | MEDLINE | ID: mdl-21813927

ABSTRACT

Myotonic dystrophy is an autosomal dominant neuromuscular disorder characterised by extreme pleiotropism and variability in disease expression. A congenital form is rare and is observed in infants born to symptomatic mothers with multisystem involvement. We report a case of a neonate with congenital myotonic dystrophy born to an asymptomatic mother.


Subject(s)
Myotonic Dystrophy/diagnosis , Myotonic Dystrophy/genetics , Blotting, Southern , Electromyography , Fathers , Female , Humans , Infant, Newborn , Infant, Premature , Male , Mothers
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