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Myotonic Dystrophy
Myotonic dystrophy
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Muscular dystrophy
(19)
Becker muscular dystrophy
Congenital muscular dystrophy
Duchenne muscular dystrophy
Dystrophin
Emery-Dreifuss muscular dystrophy
Emery-Dreifuss muscular dystrophy
Facioscapulohumeral muscular dystrophy
MD CARE Act
Oculopharyngeal muscular dystrophy
Biostrophin
Darius Goes West
Fukuyama congenital 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...
Disability
Neurological disorders
Spinocerebellar ataxia
Fragile x syndrome
Muscular dystrophy
Neurology
Limb girdle muscular dystrophy
Muscle weakness
Myasthenia gravis
Muscular dystrophy
Neurological disorders
Genetic disorders
(31)
Metachromatic leukodystrophy
Myotonia congenita
Periodic paralysis
Monosomy
Spinal muscular atrophy
Spinal muscular atrophy
Clawhand
Friedreich ataxia
Congenital myopathies
Spinocerebellar ataxia type-6
Episodic ataxia
Mucopolysa- ccharidosis
Bethlem myopathy
Aicardi syndrome
Central core disease
Rubinstein-taybi syndrome
Zaspopathy
Peutz-jeghers syndrome
Spinal muscular atrophy type 1
Galactosialidosis
Krabbe disease
Charcot-Marie-Tooth disease, type 4
Trinucleotide repeat disorders
Facioscapulohumeral muscular dystrophy
Muscular dystrophy
Congenital muscular dystrophy
Becker muscular dystrophy
Duchenne muscular dystrophy
Emery-Dreifuss muscular dystrophy
Spinocerebellar ataxia
Oculopharyngeal muscular dystrophy
Fragile x syndrome
more...
Medical condition
(41)
Myotonic dystrophy type 2
Proximal myotonic dystrophy
Myopathies
Distal muscular dystrophy
Hypotonia
Hypotonia
X-linked mental retardation
Multiple hamartoma syndrome
Riley-Day syndrome
Morvan disease
Myositis
Dystrophinopathy
Centronuclear myopathy
Floating harbor syndrome
Myotonia atrophica
Male turner syndrome
Marinesco sjogren syndrome
Dermatomyositis
Moebius syndrome
Polymyositis
Myoglobinuria
Facioscapulohumeral muscular dystrophy
Limb girdle muscular dystrophy
Muscular dystrophy
Congenital muscular dystrophy
Becker muscular dystrophy
Duchenne muscular dystrophy
Oculopharyngeal muscular dystrophy
Metachromatic leukodystrophy
Periodic paralysis
Spinal muscular atrophy
Clawhand
Friedreich ataxia
Congenital myopathies
Mucopolysa- ccharidosis
Myasthenia gravis
Bethlem myopathy
Fragile x syndrome
Central core disease
Spinal muscular atrophy type 1
Krabbe disease
Charcot-Marie-Tooth disease, type 4
more...
Muscular dystrophy organizations
Muscular Dystrophy Association
Muscular Dystrophy Campaign
Muscular Dystrophy Canada
Myotonic Dystrophy Foundation
Muscular Dystrophy Family Foundation
NeuroMuscular Centre
Diseases and disorders
(18)
Myotonia
Abnormal gait
Scissors gait
Propulsive gait
Spastic gait
Spastic gait
Steppage gait
Muscular dystrophy
Congenital muscular dystrophy
Neurological disorders
Metachromatic leukodystrophy
Distal muscular dystrophy
Multiple hamartoma syndrome
Bethlem myopathy
Myositis
Zaspopathy
Galactosialidosis
Krabbe disease
Myoglobinuria
more...
Muscular disorders
(23)
Arthrogryposis
Central core disease
Centronuclear myopathy
Chronic progressive external ophthalmoplegia
Congenital myopathies
Congenital myopathies
Diastasis recti
Inclusion body myositis
Laminopathy
Macrophagic myofasciitis
Metabolic myopathy
Mitochondrial myopathy
Muscular dystrophy
Myokmia
Myopathies
Nemaline myopathy
Orofacial myological disorders
Pelvic Floor Muscle Disorder
Polymyositis
Thyrotoxic myopathy
Torticollis
Writer's cramp
X-linked myotubular myopathy
Zenker's degeneration
more...
Muscular system
Muscle biopsy
Muscular diseases
Muscle diseases
Contractures
Dystrophin
Muscular disorders
Muscle weakness
Lysosomal storage diseases
(40)
Alpha-mannosidosis
Aspartylgl- ucosaminuria
Batten disease
Canavan disease
Cholesteryl ester storage disease
Cholesteryl ester storage disease
Cystinosis
Fabry disease
Farber disease
GM1 gangliosidoses
GM2 gangliosidoses
Galactosialidosis
Gangliosidosis
Gaucher's disease
Glycogen storage disease type II
Glycoproteinosis
Hunter syndrome
Hurler syndrome
I-cell disease
Krabbe disease
Lipid storage disorder
Lysosomal storage disease
Metachromatic leukodystrophy
Morquio syndrome
Mucolipidosis
Mucolipidosis type IV
Mucopolysa- ccharidosis
Multiple sulfatase deficiency
Neuronal ceroid lipofuscinosis
Niemann-Pick disease, type C
Niemann–Pick disease
Pseudo-Hurler polydystrophy
Pycnodysostosis
Salla disease
Sandhoff disease
Sanfilippo syndrome
Schindler disease
Sialidosis
Sly syndrome
Tay-Sachs disease
Wolman disease
more...
Symptoms
Decreased muscle tone
Frequent falls
Ptosis (eyelid)
Muscle atrophy
Myotonia
Muscle weakness
Hypotonia
See also
(20)
DM1
Gene
Dreifuss
ZNF9
ExtenZe
ExtenZe
Charles Thornton (cricketer)
Myoneural junction
Autosomal dominant
Autosomal recessive
Chloride channel
X-linked recessive
Ethotoin
Organophosphate poisoning
Mephenytoin
Anticipation (genetics)
Chromosome 3 (human)
Chromosome 19
MYO-029
Skin lightening
IPLEX
more...
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