Kosmix
One sec... we're building your guide for
Congenital Myopathies
Congenital myopathies
Overview
Treatments
Anatomy
From Experts
Patient Experiences
Video
Images
News & Blogs
More
Guides & Articles
Reference
Medical Journals
Main ›
Treatments ›
Anatomy ›
From Experts ›
Patient Experiences ›
Video ›
Images ›
News & Blogs ›
Guides & Articles ›
Reference ›
Medical Journals ›
Anatomy
›
Body Maps
Layers:
(click to view/hide)
+
Zoom
-
Search:
Related in the Kosmos
?
Muscular disorders
(22)
Arthrogryposis multiplex congenita
Central core disease
Inclusion body myositis
Mitochondrial myopathies
Muscular dystrophies
Muscular dystrophies
Myopathies, structural, congenital
Myotubular myopathy
Nemaline myopathy
Polymyositis
Thyrotoxic Myopathy
X-linked myotubular myopathy
Chronic progressive external ophthalmoplegia
Diastasis recti
Laminopathy
Macrophagic myofasciitis
Metabolic myopathy
Myokmia
Orofacial myological disorders
Pelvic Floor Muscle Disorder
Torticollis
Writer's cramp
Zenker's degeneration
more...
Genetic disorders
(23)
Hyperostosis, cortical, congenital
Adrenoleuk- odystrophy
Hereditary sensory and autonomic neuropathies
Leukodystrophy, globoid cell
Duchenne muscular dystrophy
Duchenne muscular dystrophy
Galactosemias
Bethlem myopathy
Congenital muscular dystrophies
Periodic paralyses
Spinal muscular atrophy
Facioscapulohumeral muscular dystrophy
Becker muscular dystrophy
Oculopharyngeal muscular dystrophy
Mucolipidoses
Myotonic muscular dystrophy
Acid maltase deficiency
Paramyotonia congenita
Hypokalemic periodic paralysis
Emery-Dreifuss muscular dystrophy
Mitochondrial disorders
Nemaline myopathy
Central core disease
Muscular dystrophies
more...
Diseases and disorders
(63)
Congenital fiber type disproportion
Multicore disease
Minicore disease
Glossopharyngeal nerve diseases
Purpura, schoenlein-henoch
Purpura, schoenlein-henoch
Type i complex regional pain syndrome
Intervertebral disk displacement
Enterocolitis, pseudomembranous
Physiologic nystagmus
Fetofetal transfusion
Histiocytosis non-langerhans-cell
Rigid spine syndrome
Lupus erythematosus, cutaneous
Postpoliomyelitis syndrome
Polyendocr- inopathies, autoimmune
Encephalitis, arbovirus
Olfaction disorders
Rosenthal syndrome
Brachial plexus neuropathies
Optic neuropathy, ischemic
Myopathy myotubular
Limb-girdle muscular dystrophies
Myositis inclusion body
Myositis
Inflammatory myopathy
Dermatomyositis
Myositis ossificans
Myoadenylate deaminase deficiency
Distal myopathy
Glycogen storage diseases
Myasthenia gravis
Polymyosit- is-dermatomyositis
Ophthalmoplegia
Hypotonia
Peripheral Neuropathies
Malignant hyperthermia
Amyotrophic lateral sclerosis
Myopathies, structural, congenital
Myotubular myopathy
Nemaline myopathy
Mitochondrial myopathies
Central core disease
Muscular dystrophies
Hyperostosis, cortical, congenital
Hereditary sensory and autonomic neuropathies
Leukodystrophy, globoid cell
Duchenne muscular dystrophy
Polymyositis
Galactosemias
Bethlem myopathy
X-linked myotubular myopathy
Congenital muscular dystrophies
Periodic paralyses
Spinal muscular atrophy
Facioscapulohumeral muscular dystrophy
Becker muscular dystrophy
Oculopharyngeal muscular dystrophy
Mucolipidoses
Myotonic muscular dystrophy
Acid maltase deficiency
Paramyotonia congenita
Arthrogryposis multiplex congenita
Hypokalemic periodic paralysis
more...
Neurological disorders
Neuromyotonia
Nemaline myopathy
Central core disease
Hereditary sensory and autonomic neuropathies
Olfaction disorders
Paramyotonia congenita
Peripheral Neuropathies
Autosomal recessive disorders
Nemaline myopathy
Leukodystrophy, globoid cell
Mucolipidoses
Acid maltase deficiency
Neurology
(8)
Muscle weakness
Muscular dystrophies
Adrenoleuk- odystrophy
Limb-girdle muscular dystrophies
Myotonic muscular dystrophy
Myotonic muscular dystrophy
Myasthenia gravis
Ophthalmoplegia
Mitochondrial disorders
more...
Muscular system
Neuromuscular disease
Muscle biopsy
Muscle cells
Skeletal muscle
Tropomyosin
Motor neuron disease
(11)
ALS Association
ALS Society of Canada
Amyotrophic lateral sclerosis
Monomelic amyotrophy
Motor neurone disease
Motor neurone disease
People with motor neuron disease
Postpoliomyelitis syndrome
Primary lateral sclerosis
Spinal muscular atrophy
Split hand syndrome
Survival motor neuron spinal muscular atrophy
more...
Skeletal muscle
Myosin
Neuromuscular
Muscle contraction
Muscle cross-sectional area
Sliding filament model
Disorders of muscles
(8)
Muscular disorders, atrophic
Compartment syndrome
Contracture
Fibrodysplasia ossificans progressiva
Myositis
Myositis
Myositis ossificans
Pyomyositis
Strain (injury)
more...
Proteins
SEPN1
Dysferlin
Nebulin
Selenoprotein
Myosin
Gene
ACTA1
TPM3
Merosin
Dysferlin
Nebulin
Symptoms
Facial weakness
Skeletal deformities
Respiratory failure
Muscle weakness
Muscular disorders, atrophic
Hypotonia
Muscular dystrophy
(21)
Becker muscular dystrophy
Biostrophin
Congenital muscular dystrophies
Darius Goes West
Duchenne muscular dystrophy
Duchenne muscular dystrophy
Dystrophin
Emery-Dreifuss muscular dystrophy
Facioscapulohumeral muscular dystrophy
Fukuyama congenital muscular dystrophy
Help Cure Muscular Dystrophy
Jerry Lewis MDA Telethon
Laminopathy
Moonrise (Penny Wolfson book)
Muscular Dystrophy Community Assistance Research and Education Amendments of 2001
Muscular dystrophy organizations
Myostatin
Myotonic muscular dystrophy
Oculopharyngeal muscular dystrophy
People with muscular dystrophy
Robert Ross (CEO)
Walker-Warburg syndrome
more...
See also
(13)
RyR1
Autosomal dominant
Autosomal recessive
FKRP
Muscular Dystrophy Association
Muscular Dystrophy Association
Bulbar
Congenital
Alpha-actin
Myotubularin
Myofibrillar
Erik Pettersson (bandy player)
James M. Beggs
Mutations
more...
more categories...
Health Providers & Organizations
›
Vitals.com
