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Muscular Dystrophy - Duchenne Type
Muscular dystrophy - Duchenne type
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Muscular dystrophy
(20)
Becker muscular dystrophy
Congenital muscular dystrophy
Dystrophin
Emery-Dreifuss muscular dystrophy
Facioscapulohumeral muscular dystrophy
Facioscapulohumeral muscular dystrophy
Fukuyama type muscular dystrophy
MD CARE Act
Myotonic dystrophy
Oculopharyngeal muscular dystrophy
Biostrophin
Darius Goes West
Help Cure Muscular Dystrophy
Jerry Lewis MDA Telethon
Laminopathy
Moonrise (Penny Wolfson book)
Muscular dystrophy organizations
Myostatin
People with muscular dystrophy
Robert Ross (CEO)
Walker-Warburg syndrome
more...
Genetic disorders
(23)
Mucopolysa- ccharidosis
Clawhand
Gaucher disease
Spinal muscular atrophy type 1
Spinal muscular atrophy
Spinal muscular atrophy
Alexander disease
McArdle syndrome
Spinocerebellar ataxia
Charcot-Marie-Tooth disease, type 4
Spondyloep- imetaphyseal dysplasia, Strudwick type
Multiple sulfatase deficiency
Bethlem myopathy
Dejerine-Sottas disease
Trisomy
Nemaline myopathy
Muscular dystrophies
Myotonic dystrophy
Becker muscular dystrophy
Facioscapulohumeral muscular dystrophy
Emery-Dreifuss muscular dystrophy
Congenital muscular dystrophy
Fukuyama type muscular dystrophy
Oculopharyngeal muscular dystrophy
more...
Diseases and disorders
(45)
Myotonic
Myopathies
Limb-girdle muscular dystrophies
Complex regional pain syndrome
Distal muscular dystrophy
Distal muscular dystrophy
Dystrophinopathy
Cardiomyopathy
Mitochondrial myopathy
Mesangiocapillary glomerulonephritis
Metatropic dwarfism
Metrorrhagia
Ehlers-danlos syndrome dermatosparaxis type
Myotonic dystrophy type 2
Morvan disease
Ectodermal dysplasia
Megarectum
Meningococcal
Myelomeningocele
Scoliosis
Medulloblastoma
Marinesco sjogren syndrome
Diencephalic syndrome
Macrocephaly
Aplasia
Decubitus ulcers
Myotubular myopathy
Glycogen storage disease
Muscular dystrophies
Myotonic dystrophy
Becker muscular dystrophy
Facioscapulohumeral muscular dystrophy
Mucopolysa- ccharidosis
Clawhand
Congenital muscular dystrophy
Fukuyama type muscular dystrophy
Oculopharyngeal muscular dystrophy
Gaucher disease
Spinal muscular atrophy type 1
Spinal muscular atrophy
Alexander disease
Charcot-Marie-Tooth disease, type 4
Spondyloep- imetaphyseal dysplasia, Strudwick type
Multiple sulfatase deficiency
Bethlem myopathy
Nemaline myopathy
more...
Medical terms
Age of onset
Neuronopathy
Diseases and disorders
Muscular disorders
(23)
Arthrogryposis
Central core disease
Chronic progressive external ophthalmoplegia
Congenital myopathy
Diastasis recti
Diastasis recti
Inclusion body myositis
Laminopathy
Macrophagic myofasciitis
Metabolic myopathy
Mitochondrial myopathy
Muscular dystrophies
Myokmia
Myopathies
Myotubular myopathy
Nemaline myopathy
Orofacial myological disorders
Pelvic Floor Muscle Disorder
Polymyositis
Thyrotoxic myopathy
Torticollis
Writer's cramp
X-linked myotubular myopathy
Zenker's degeneration
more...
Disability
Muscular dystrophies
Myotonic dystrophy
Spinocerebellar ataxia
Myelomeningocele
Neurology
Muscle weakness
Electromyography
Muscular dystrophies
Myotonic dystrophy
Limb-girdle muscular dystrophies
Medulloblastoma
Neuronopathy
Cytoskeleton
Utrophin
Spectrin
Dystrophin
Muscular system
Muscle biopsy
Muscle diseases
Muscle cells
Muscle fibres
Dystrophin
Muscular disorders
Muscular dystrophy organizations
Muscular Dystrophy Association
Muscular Dystrophy Canada
Myotonic Dystrophy Foundation
Muscular Dystrophy Campaign
Muscular Dystrophy Family Foundation
NeuroMuscular Centre
Genetics
X-linked recessive
X linked
Mutation
Introduction to genetics
Genetic disorders
Symptoms
(8)
Progressive difficulty walking
Contractures of heels legs
Pseudohypertrophy of calf muscles
Muscle deformities
Muscle wasting
Muscle wasting
Difficulty walking
Fatigue
Muscle weakness
more...
Gene
Dysferlin
GM2A
DM1
Merosin
Causes, incidence, and risk factors
Muscle contractures
Protein
Wasting
Muscular dystrophy
Becker's muscular dystrophy
Cardiomyopathy
Signs and tests
(9)
Aspiration
Cardiac arrhythmia
EMG
Heart failure
Pneumonia
Pneumonia
Respiratory system
Serum CPK
Muscle biopsy
Cardiomyopathy
more...
See also
(20)
Contractures
Midface trauma
Creatine kinase
Myoblasts
Voluntary muscles
Voluntary muscles
Nonsense mutations
Morpholino
Muscular dystrophy - support group
Stress
Support group
Sarcoglycans
MYO-029
Autosomal recessive
MDCC
Autosomal dominant
Myoneural junction
Muscle glycogen phosphorylase
Point mutation
Anemia, macrocytic
Corneal dystrophy
more...
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