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Spinal and Bulbar Muscular Atrophy
Spinal and bulbar muscular atrophy
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Neurological disorders
(13)
X-linked mental retardation and macroorchidism
Hereditary sensory and autonomic neuropathies
Fazio-Londe disease
Olfaction disorders
Motor neurone disease
Motor neurone disease
Motor neuron disease
Infantile spasm
Congenital myasthenic syndrome
Trinucleotide repeat
Spinocerebellar ataxia
Dysarthria
Polyneuropathy
DRPLA
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Disability
X-linked mental retardation and macroorchidism
Motor neurone disease
Spinocerebellar ataxia
Dysarthria
Endocrinology
Polyendocr- inopathies, autoimmune
XO syndrome
Genetic disorders
(30)
Spinal muscular atrophy
Kugelberg-Welander syndrome
Androgen insensitivity
Spondyloep- imetaphyseal dysplasia, Strudwick type
Hyperostosis, cortical, congenital
Hyperostosis, cortical, congenital
Adrenoleuk- odystrophy
Spondyloperipheral dysplasia
Leukodystrophy, globoid cell
XXXXX syndrome
XXY syndrome
Galactosemias
X-linked sideroblastic anemia
Kniest dysplasia
47 xyy syndrome
SCAD deficiency
Spondyloepiphyseal dysplasia
XLSA
Duchenne muscular dystrophy
Stickler syndrome
X-linked severe combined immunodeficiency
Congenital myopathy
SADDAN
Smith-Magenis syndrome
X-linked mental retardation and macroorchidism
Hereditary sensory and autonomic neuropathies
Fazio-Londe disease
XO syndrome
Trinucleotide repeat
Spinocerebellar ataxia
DRPLA
more...
Diseases and disorders
(62)
Spinal bulbar muscular atrophy
Progressive bulbar palsy
Progressive muscular atrophy
Bulbospinal neuronopathy
Myopathies, structural, congenital
Myopathies, structural, congenital
Glossopharyngeal nerve diseases
Purpura, schoenlein-henoch
Type i complex regional pain syndrome
Postpoliomyelitis syndrome
Enterocolitis, pseudomembranous
Physiologic nystagmus
Fetofetal transfusion
Histiocytosis non-langerhans-cell
Xeroderma pigmentosum variant type
Severe achondroplasia with developmental delay and acanthosis nigricans
Lupus erythematosus, cutaneous
Encephalitis, arbovirus
Primary lateral sclerosis
Bulbar palsy
Brachial plexus neuropathies
Intervertebral disk displacement
Syndromes
Rosenthal syndrome
Amyotrophic lateral sclerosis
Alzheimer disease type 2
X-linked retinoschisis
Optic neuropathy, ischemic
Spongioblastoma
Pseudobulbar palsy
X-linked lymphoproliferative syndrome
Hypospadias
X-linked hypophosphatemia
Myotonic dystrophy type 2
Sotos syndrome
Fasciculations
Poliomyelitis
Centronuclear myopathy
Mastodynia
Spinal muscular atrophy
Kugelberg-Welander syndrome
Androgen insensitivity
X-linked mental retardation and macroorchidism
Spondyloep- imetaphyseal dysplasia, Strudwick type
Hyperostosis, cortical, congenital
Hereditary sensory and autonomic neuropathies
Fazio-Londe disease
Leukodystrophy, globoid cell
Polyendocr- inopathies, autoimmune
Olfaction disorders
Motor neurone disease
XXY syndrome
Galactosemias
X-linked sideroblastic anemia
Kniest dysplasia
Infantile spasm
47 xyy syndrome
Spondyloepiphyseal dysplasia
XLSA
Duchenne muscular dystrophy
Stickler syndrome
Congenital myopathy
Polyneuropathy
more...
Motor neuron disease
(11)
ALS Association
ALS Society of Canada
Amyotrophic lateral sclerosis
Kugelberg-Welander syndrome
Monomelic amyotrophy
Monomelic amyotrophy
Motor neurone disease
People with motor neuron disease
Postpoliomyelitis syndrome
Primary lateral sclerosis
Spinal muscular atrophy
Split hand syndrome
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Efferent neurons
Lower motor neurons
Motor neuron
Upper motor neurons
Alpha motor neuron
Gamma motoneuron
Somatic motor system
(13)
Motor unit
Alpha motor neuron
Bereitscha- ftspotential
Lower motor neurons
Memory Cells (Motor Cortex)
Memory Cells (Motor Cortex)
Motor cortex
Motor unit recruitment
Neuromuscular junction
Primary motor cortex
Skeletal muscle
Stretch reflex
Supplementary motor area
Upper motor neurons
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Neuroanatomy
Bulbar
Anterior horn cells
Axonal
Lower motor neurons
Neurology
Neuronopathy
Electromyography
Muscle weakness
Adrenoleuk- odystrophy
Spongioblastoma
See also
(20)
Androgen receptor
X linked
Bulbospinal
Complete androgen insensitivity
Polyglutamine tract
Polyglutamine tract
Muscular atrophy
Anatomy
Peripheral nerve
ALS2
Androgens
Dihydrotestosterone
X-linked adrenal hypoplasia congenita
X-linked spinal muscular atrophy 2
Exsufflation
Neuromuscular disease
Muscular Dystrophy Association
X-linked recessive
Nuclear receptor
Bulbar polio
Testicular atrophy
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