Spinal muscular atrophy (SMA) is a rare neuromuscular disorder that results in the loss of motor neurons and progressive muscle wasting. It is usually...
90 KB (10,015 words) - 03:08, 25 November 2024
Congenital distal spinal muscular atrophy (cDSMA), also known as distal hereditary motor neuropathy (or neuronopathy) type VIII (dHMN8), is a hereditary...
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muscles; Distal spinal muscular atrophies (which significantly overlap with distal hereditary motor neuronopathies) where they affect primarily distal muscles...
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hypertrophy Muscular Dystrophy UK Muscular Dystrophy Association (United States) Muscular Dystrophy Canada Spinal muscular atrophies "NINDS Muscular Dystrophy...
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Hirayama disease (redirect from Juvenile muscular atrophy of the distal upper limb)
Tokumaru, Y. (23 May 2000). "Cervical dural sac and spinal cord in juvenile muscular atrophy of distal upper extremity". Neurology. 54 (10): 1922–1926. doi:10...
19 KB (2,254 words) - 09:12, 19 July 2024
Arthrogryposis (redirect from Arthrogryposis spinal muscular atrophy)
multiplex congenita distal (AMCD), also known as X-linked spinal muscular atrophy type 2. Gordon syndrome, also known as distal arthrogryposis type 3...
35 KB (3,588 words) - 19:20, 22 July 2024
system of classification groups many of DHMNs under the heading of spinal muscular atrophies.[citation needed] In 1993, A. E. Hardnig proposed to classify...
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Complex regional pain syndrome Compression neuropathy Congenital distal spinal muscular atrophy Congenital facial diplegia Color blindness Cornelia de Lange...
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ALS (redirect from Primary muscular atrophy)
neurons in the spinal cord. Primary lateral sclerosis (PLS) involves degeneration of only the upper motor neurons, and progressive muscular atrophy (PMA) involves...
129 KB (13,979 words) - 20:44, 22 December 2024
Tetraplegia (redirect from Spinal paralysis)
Guillain–Barré syndrome, multiple sclerosis, or polio), or congenital disorders (such as muscular dystrophy). Tetraplegia is defined in many ways; C1–C4 usually...
30 KB (3,199 words) - 01:39, 11 November 2024
peripheral nervous system. Amyotrophic lateral sclerosis Spinal muscular atrophy Spinal muscular atrophy with respiratory distress type 1 Atypical motor neuron...
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Clubfoot (redirect from Congenital talipes equinovarus)
abnormalities: arthrogryposis multiplex congenita, myotonic dystrophy, spinal muscular atrophy, neural tube defects, holoprosencephaly, and hydranencephaly. Clubfoot...
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muscular dystrophy (BMD), congenital muscular dystrophies (CMD), myotonic dystrophy (DM), spinal muscular atrophy (SMA), and myasthenia gravis (MG). MDA...
47 KB (4,963 words) - 02:21, 22 December 2024
DSMA may refer to: Congenital distal spinal muscular atrophy (congenital dSMA), a hereditary condition characterized by muscle wasting Defence and Security...
1 KB (173 words) - 19:21, 6 August 2024
nasal tip Spinal and bulbar muscular atrophy (SBMA), also known as Kennedy's disease; muscle cramps and progressive weakness Spinal muscular atrophy caused...
15 KB (1,754 words) - 13:41, 12 August 2024
type 3, congenital distal spinal muscular atrophy, Familial digital arthropathy-brachydactyly (FDAB), scapuloperoneal spinal muscular atrophy, and subtype...
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syndrome 1 Infantile neuroaxonal dystrophy Infantile-onset X-linked spinal muscular atrophy Intellectual developmental disorder, autosomal dominant 64, 65...
15 KB (1,484 words) - 03:37, 9 December 2024
Syndrome". "Distal Myopathies - Types of Distal MD". Muscular Dystrophy Association. 2015-12-18. Retrieved 2019-04-16. "OMIM Entry - # 310200 - MUSCULAR DYSTROPHY...
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neoplasm Spinal dysostosis type Anhalt Spinal muscular atrophy Spinal muscular atrophy with congenital bone fractures Spinal muscular atrophy with lower...
23 KB (1,934 words) - 08:11, 11 December 2024
Arthrogryposis renal dysfunction cholestasis syndrome Arthrogryposis spinal muscular atrophy Arylsulfatase A deficiency Asbestosis Ascariasis Ascher's syndrome...
24 KB (1,972 words) - 21:28, 16 August 2024
Carmen; Torrelo, Antonio; López-Gutiérrez, Juan C. (June 2021). "Congenital Aberrant Muscular Overgrowth of Hands and Feet in Patients With PIK3CA Overgrowth...
85 KB (5,216 words) - 15:17, 2 December 2024
Ehlers–Danlos syndrome (category Congenital disorders)
(mEDS), is characterized by three major criteria: congenital muscle hypotonia and/or muscle atrophy that improves with age, proximal joint contractures...
112 KB (11,789 words) - 06:50, 22 December 2024
Congenital benign spinal muscular atrophy dominant Congenital brain disorder Congenital bronchobiliary fistula Congenital c – Congenital g Congenital cardiovascular...
40 KB (3,657 words) - 03:02, 17 August 2024
short stature Lumbar spinal stenosis Lundberg syndrome Lung agenesis heart defect thumb anomalies Lung cancer Lung herniation congenital defect of sternem...
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Olivopontocerebellar atrophy deafness Olivopontocerebellar atrophy type 1 Olivopontocerebellar atrophy type 2 Olivopontocerebellar atrophy type 3 Olivopontocerebellar...
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pallidum Spinal cord injury Myelomeningocele Syringomyelia Intra-articular steroid injections Congenital insensitivity to pain Peroneal muscular atrophy Two...
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urethra. The proximal parts of the corpus spongiosum form the bulb and the distal ends form the glans penis. The enlarged and bulbous-shaped end of the corpus...
65 KB (7,441 words) - 19:35, 13 December 2024
determined primarily by the type of scoliosis encountered: syndromic, congenital, neuromuscular, or idiopathic. Treatment options for idiopathic scoliosis...
62 KB (7,656 words) - 01:13, 25 September 2024
weakness and atrophy of the distal extremities (mostly involving feet, legs, and the thenar eminence of the hands), loss of sensation of the distal limbs, loss...
16 KB (1,756 words) - 11:03, 25 August 2023
Neurological conditions linked to RLS include Parkinson's disease, spinal cerebellar atrophy, spinal stenosis,[specify] lumbosacral radiculopathy and Charcot–Marie–Tooth...
79 KB (8,406 words) - 14:03, 17 December 2024