Histometric data on muscle fiber types were studied in two cases of congenital myotonic dystrophy (CMD); one underwent biopsy at the age of 5 months and the other at the age of 10 years. A previously unreported severe deficiency of type IIB fibers were found in both cases. In addition, in the first case, there was type I fiber preponderance and hypotrophy as described in cases of congenital fiber type disproportion (CFTD). It is suggested that an abnormality of motor unit maturation may be common to CMD and to CFTD, and that this results from a disorder of neural trophic influences during muscle developmen
The clinical features of myotonic dystrophy type 1 (DM1) and type 2 (DM2) may present striking simil...
The congenital muscular dystrophies (CMD) are a clinically and genetically heterogeneous group of ne...
Congenital fibre type disproportion (CFTD) is a histological abnormality characterized by small type...
The histopathology of biopsied skeletal muscles and clinical findings were studied in 15 patients wi...
Congenital fiber type disproportion is a rare type of congenital myopathy which presents as hypotoni...
AbstractCongenital fiber-type disproportion myopathy causes impaired muscle maturation or developmen...
Muscle biopsies from quadriceps femoris muscle of normal subjects and subjects with symptoms of cong...
Congenital muscular dystrophies (CMDs) are a wide group of muscular disorders that manifest with ver...
We studied the histochemical characteristics of muscle in five hypotonic infants. A number of differ...
Congenital myopathies are clinical and genetic heterogeneous disorders characterized by skeletal mus...
Congenital fiber-type disproportion myopathy causes impaired muscle maturation or development. It is...
Introduction. An accurate assessment of clinical presentation and genetic causes of congenital muscu...
Myotonic dystrophy (DM) is the most common muscular dystrophy in adults. Two known genetic subtypes ...
Congenital muscular dystrophies (CMDs) are a wide group of muscular disorders that manifest with ver...
Congenital myopathies form a clinically, genetically, and morphologically heterogeneous group of neu...
The clinical features of myotonic dystrophy type 1 (DM1) and type 2 (DM2) may present striking simil...
The congenital muscular dystrophies (CMD) are a clinically and genetically heterogeneous group of ne...
Congenital fibre type disproportion (CFTD) is a histological abnormality characterized by small type...
The histopathology of biopsied skeletal muscles and clinical findings were studied in 15 patients wi...
Congenital fiber type disproportion is a rare type of congenital myopathy which presents as hypotoni...
AbstractCongenital fiber-type disproportion myopathy causes impaired muscle maturation or developmen...
Muscle biopsies from quadriceps femoris muscle of normal subjects and subjects with symptoms of cong...
Congenital muscular dystrophies (CMDs) are a wide group of muscular disorders that manifest with ver...
We studied the histochemical characteristics of muscle in five hypotonic infants. A number of differ...
Congenital myopathies are clinical and genetic heterogeneous disorders characterized by skeletal mus...
Congenital fiber-type disproportion myopathy causes impaired muscle maturation or development. It is...
Introduction. An accurate assessment of clinical presentation and genetic causes of congenital muscu...
Myotonic dystrophy (DM) is the most common muscular dystrophy in adults. Two known genetic subtypes ...
Congenital muscular dystrophies (CMDs) are a wide group of muscular disorders that manifest with ver...
Congenital myopathies form a clinically, genetically, and morphologically heterogeneous group of neu...
The clinical features of myotonic dystrophy type 1 (DM1) and type 2 (DM2) may present striking simil...
The congenital muscular dystrophies (CMD) are a clinically and genetically heterogeneous group of ne...
Congenital fibre type disproportion (CFTD) is a histological abnormality characterized by small type...