American Journal of Medical Genetics · 1989 · 59 citations · 17 references
MedicineNeurologyPediatricsMovement DisordersNeuromuscular DisordersPediatric NeurologyMuscle DisordersMuscular DystrophyPediatric Movement DisordersSpinal Muscular AtrophyInfantile Spinal Muscular AtrophyPediatric Muscle WeaknessPediatric Neuromuscular DisordersPediatric Spinal Muscular Atrophy
We report the clinical, electrophysiological, and morphological observations of five infants with an unusual form of spinal muscular atrophy (SMA). In these infants muscular weakness and atrophy were initially restricted to the distal limbs and this pattern was associated with paralysis of the diaphragm. The difference between the clinical manifestations of this syndrome and the classical form of infantile spinal muscular atrophy (SMA type 1) as well as other congenital hereditary neuropathies is discussed.
17
CLASSIFICATION OF SPINAL MUSCULAR ATROPHIES
John Pearn · The Lancet · 1980 · 426 citations
M. Bjørneboe, Hanne Prytz · The Lancet · 1975 · 302 citations
Medicine, Immunology, Pathology +12
Hereditary distal spinal muscular atrophy
A. E. Harding, P. K. Thomas · Journal of the Neurological Sciences · 1980 · 145 citations
Life Sciences, Genetics, Neurology +10
CONGENITAL HYPOMYELINATION POLYNEUROPATHY
G. Ferrière, G Lyon · Brain · 1982 · 90 citations