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Facioscapulohumeral Muscular Dystrophy
Facioscapulohumeral muscular dystrophy
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Muscular dystrophy
(19)
Becker's muscular dystrophy
Congenital muscular dystrophy
Duchenne muscular dystrophy
Dystrophin
Emery-Dreifuss muscular dystrophy
Emery-Dreifuss muscular dystrophy
Fukuyama type muscular dystrophy
MD CARE Act
Muscular dystrophy organizations
Myostatin
Myotonic dystrophy
Oculopharyngeal muscular dystrophy
Biostrophin
Darius Goes West
Jerry Lewis MDA Telethon
Laminopathy
Moonrise (Penny Wolfson book)
People with muscular dystrophy
Robert Ross (CEO)
Walker-Warburg syndrome
more...
Genetic disorders
(25)
Familial spastic paraparesis
Fibrous dysplasia of bone
Fibromuscular dysplasia
Clawhand
Spinal muscular atrophy
Spinal muscular atrophy
Familial paroxysmal polyserositis
Bethlem myopathy
Carnitine Palmityl Transferase Deficiency
Zaspopathy
Dejerine-Sottas disease
Familial periodic paralysis
Fabry disease
Multiple sulfatase deficiency
Charcot-Marie Tooth Disease
Central core disease
Myotonia congenita
Fanconi anemia
Muscular dystrophy
Myotonic dystrophy
Duchenne muscular dystrophy
Becker's muscular dystrophy
Oculopharyngeal muscular dystrophy
Emery-Dreifuss muscular dystrophy
Congenital muscular dystrophy
Fukuyama type muscular dystrophy
more...
Medical condition
(51)
Fasciitis, necrotizing
Floppy mitral valve
Myopathies
Familial dysbetalip- oproteinemia
Fibromyoma
Fibromyoma
Factor v deficiency
Factor x deficiency
Fish tapeworm
Limb girdle muscular dystrophy
Fibrosing alveolitis
Factor vii deficiency
Complex regional pain syndrome
Distal muscular dystrophy
Fast breathing
Mitochondrial myopathies
Fg syndrome
Fatty oxidation disorder
Fiber type disproportion congenital
Fetal aids infection
Factor V Leiden thrombophilia
Morvan disease
Metatropic dwarfism
Gouty nephropathy familial
Fibrocystic breast disease
Fibromyositis
Sciatic nerve dysfunction
Frambesia tropica
Myotubular myopathy
Polymyositis
Marinesco sjogren syndrome
Fifth disease
Muscular dystrophy
Myotonic dystrophy
Duchenne muscular dystrophy
Familial spastic paraparesis
Fibrous dysplasia of bone
Becker's muscular dystrophy
Oculopharyngeal muscular dystrophy
Fibromuscular dysplasia
Congenital muscular dystrophy
Clawhand
Fukuyama type muscular dystrophy
Spinal muscular atrophy
Familial paroxysmal polyserositis
Bethlem myopathy
Carnitine Palmityl Transferase Deficiency
Familial periodic paralysis
Fabry disease
Charcot-Marie Tooth Disease
Central core disease
Fanconi anemia
more...
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 myopathies
Muscular dystrophy
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...
Neurology
Muscle weakness
Electromyography
Muscular dystrophy
Myotonic dystrophy
Familial spastic paraparesis
Limb girdle muscular dystrophy
Sciatic nerve dysfunction
Muscular system
Contractures
Neuromuscular disease
Muscle biopsy
Dystrophin
Muscle weakness
Coagulation system
(34)
Factor II deficiency
Antithrombin
Bone hemostasis
Clot retraction
Coagulation
Coagulation
Cofact
Des-gamma carboxyprothrombin
Factor IX
Factor VIII
Factor XI
Factor XII
Factor XIII
Factor v deficiency
Factor vii deficiency
Factor x deficiency
Fibrin
Fibrinogenolysis
Hemostasis
High-molec- ular-weight kininogen
Human Activated Protein C
Medical Laboratory Scientist
Platelet
Platelet activation
Prekallikrein
Protein C
Protein S
Protein Z
Protein Z-related protease inhibitor
Prothrombin complex concentrate
Prothrombinase
Thrombomodulin
Tissue factor
Tissue factor pathway inhibitor
Von Willebrand factor
more...
Neurological disorders
(8)
Facial paralysis
Axillary nerve dysfunction
Complex regional pain syndrome
Zaspopathy
Dejerine-Sottas disease
Dejerine-Sottas disease
Charcot-Marie Tooth Disease
Central core disease
Myotonia congenita
more...
Muscular dystrophy organizations
Muscular Dystrophy Association
Muscular Dystrophy Canada
Muscular Dystrophy Family Foundation
Myotonic Dystrophy Foundation
Muscular Dystrophy Campaign
NeuroMuscular Centre
Symptoms
(11)
Pronounced shoulder blades
Decreased facial expression
Inability to whistle
Eyelid drooping
Difficulty pronouncing words
Difficulty pronouncing words
Angry facial expression
Muscle wasting
Facial muscle weakness
Muscle weakness
Fast breathing
Facial paralysis
more...
See also
(20)
Diseases and disorders
Familial hypertrigl- yceridemia
Myotonic
Fenestrations
MYO-029
MYO-029
Myoneural junction
Autosomal dominant
Autosomal recessive
Neuromuscular junction disease
Familial
Chromosome 4
FRG1
Creatine kinase
Creatine phosphate
Chief complaint
EMG
Genetic disorder
MedlinePlus
National Institutes of Health
Tissue (anatomy)
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