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Up to: Muscular dystrophy · Congenital nervous system disorder

Congenital muscular dystrophy

A muscular dystrophy that is characterized by diminished muscle tone (hypotonia), progressive muscle weakness and degeneration (atrophy), abnormally fixed joints, spinal rigidity, and delays in reaching motor milestones such as sitting or standing unassisted.

1 trial tagged with this condition →

Congenital merosin-deficient muscular dystrophy 1A 3 trials
Congenital muscular dystrophy due to LMNA mutation 2 trials
Congenital myasthenic syndrome 10 2 trials
Muscular dystrophy-dystroglycanopathy 0 trials · 1 incl. sub-types Sub-types →
Rigid spine syndrome 0 trials · 1 incl. sub-types Sub-types →
Bethlem myopathy 0 trials Sub-types →
SNUPN-related muscular dystrophy with or without multi-system involvement 0 trials Sub-types →
Ullrich congenital muscular dystrophy 0 trials Sub-types →
Arthrogryposis due to muscular dystrophy 0 trials
Autosomal recessive myogenic arthrogryposis multiplex congenita 0 trials
Collagen 6-related congenital muscular dystrophy 0 trials Sub-types →
Congenital muscular dystrophy 1B 0 trials
Congenital muscular dystrophy caused by variation in POMGNT2 0 trials Sub-types →
Congenital muscular dystrophy due to integrin alpha-7 deficiency 0 trials
Congenital muscular dystrophy with cataracts and intellectual disability 0 trials
Congenital muscular dystrophy with hyperlaxity 0 trials
Congenital muscular dystrophy without intellectual disability 0 trials
Congenital muscular dystrophy-infantile cataract-hypogonadism syndrome 0 trials
Congenital muscular dystrophy-respiratory failure-skin abnormalities-joint hyperlaxity syndrome 0 trials
Congenital myopathy, Paradas type 0 trials
Megaconial type congenital muscular dystrophy 0 trials
Muscle-eye-brain disease 0 trials Sub-types →
Muscular dystrophy, congenital, with rapid progression 0 trials