 | Distal spinal muscular atrophy type 1 (DSMA1), also known as spinal muscular atrophy with respiratory distress type 1 (SMARD1), is a rare neuromuscular... 16 KB (1,543 words) - 01:22, 24 March 2024 |
 | Spinal muscular atrophy (SMA) is a rare neuromuscular disorder that results in the loss of motor neurons and progressive muscle wasting. It is usually... 89 KB (9,941 words) - 10:26, 19 April 2024 |
| muscles; Distal spinal muscular atrophies (which significantly overlap with distal hereditary motor neuronopathies) where they affect primarily distal muscles... 16 KB (600 words) - 09:47, 18 March 2024 |
 | Spinal and bulbar muscular atrophy (SBMA), popularly known as Kennedy's disease, is a rare, adult-onset, X-linked recessive lower motor neuron disease... 43 KB (4,927 words) - 01:14, 8 November 2023 |
Congenital distal spinal muscular atrophy (cDSMA), also known as distal hereditary motor neuropathy (or neuronopathy) type VIII (dHMN8), is a hereditary... 9 KB (937 words) - 22:13, 11 September 2023 |
system of classification groups many of DHMNs under the heading of spinal muscular atrophies.[citation needed] In 1993, A. E. Hardnig proposed to classify... 5 KB (226 words) - 22:49, 27 March 2024 |
| Distal spinal muscular atrophy type 2 (DSMA2), also known as Jerash type distal hereditary motor neuropathy (HMNJ), is a very rare childhood-onset genetic... 3 KB (218 words) - 04:33, 23 April 2023 |
of consciousness Distal hereditary motor neuropathy type V Distal spinal muscular atrophy type 1 Distal spinal muscular atrophy type 2 Dizziness Down... 13 KB (1,145 words) - 18:16, 6 May 2024 |
 | Arthrogryposis (redirect from Arthrogryposis spinal muscular atrophy) congenita distal (AMCD), also known as X-linked spinal muscular atrophy type 2. Gordon syndrome, also known as distal arthrogryposis type 3. Arthrogryposis... 32 KB (3,457 words) - 17:57, 8 November 2023 |
 | Charcot–Marie–Tooth disease (redirect from Peroneal muscular atrophy type 1) Médicale (in French). 6: 97–138. Tooth HH (1886). The peroneal type of progressive muscular atrophy (MD thesis). London. Kumar DR, Aslinia F, Yale SH, Mazza... 40 KB (4,443 words) - 16:41, 14 March 2024 |
| Motor neuron diseases (category Systemic atrophies primarily affecting the central nervous system) (PBP), pseudobulbar palsy, progressive muscular atrophy (PMA), primary lateral sclerosis (PLS), spinal muscular atrophy (SMA) and monomelic amyotrophy (MMA)... 21 KB (2,137 words) - 12:30, 23 March 2024 |
 | muscular dystrophy Muscle hypertrophy Muscular Dystrophy UK Muscular Dystrophy Association (United States) Muscular Dystrophy Canada Spinal muscular atrophies... 28 KB (2,070 words) - 12:28, 6 April 2024 |
 | Facioscapulohumeral muscular dystrophy (FSHD) is a type of muscular dystrophy, a group of heritable diseases that cause degeneration of muscle and progressive... 174 KB (16,335 words) - 04:50, 29 April 2024 |
 | 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... 130 KB (14,009 words) - 01:59, 12 May 2024 |
 | factor 1 (CATF1) – is a protein that in humans is encoded by the IGHMBP2 gene. Mutations in the IGHMBP2 gene cause distal spinal muscular atrophy type 1 (distal... 4 KB (523 words) - 00:30, 4 March 2023 |
system. Amyotrophic lateral sclerosis Spinal muscular atrophy Spinal muscular atrophy with respiratory distress type 1 Atypical motor neuron diseases Dorsal... 9 KB (899 words) - 01:15, 30 January 2023 |
 | Tetraplegia (redirect from Spinal paralysis) touch, pressure, heat, pinprick/pain, and proprioception. In these types of spinal cord injury, it is common to have a loss of both sensation and motor... 30 KB (3,198 words) - 01:11, 10 May 2024 |
SMARD may refer to: Distal spinal muscular atrophy type 1, a rare neuromuscular disorder SMARD, a data portal provided by the German Federal Network Agency... 239 bytes (63 words) - 12:38, 24 November 2023 |
 | Mutations in the SIGMAR1 gene have been associated with distal spinal muscular atrophy type 2. The following ligands have high affinity for the σ1 receptor... 27 KB (2,960 words) - 11:04, 16 April 2024 |
Polyneuropathy in dogs and cats (redirect from Birman cat distal polyneuropathy) autosomal recessive trait. Spinal muscular atrophy occurs in cats and dogs, and is caused by the death of nerve cells in the spinal cord. This progressive... 14 KB (1,636 words) - 16:28, 11 July 2019 |
 | Ehlers–Danlos syndrome (redirect from Ehlers-Danlos syndrome, type 3) hypotonia and/or muscle atrophy that improves with age, proximal joint contractures of the knee, hip, and elbow, and hypermobility of distal joints (ankles, wrists... 109 KB (11,320 words) - 17:47, 10 May 2024 |
diseases and their caretakers. Mindy Henderson, diagnosed with type 2 spinal muscular atrophy (SMA) and a patient advocate, is the editor-in-chief as of 2023... 39 KB (4,019 words) - 18:43, 6 May 2024 |
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) - 16:05, 15 March 2024 |
Syndrome". "Distal Myopathies - Types of Distal MD". Muscular Dystrophy Association. 2015-12-18. Retrieved 2019-04-16. "OMIM Entry - # 310200 - MUSCULAR DYSTROPHY... 42 KB (969 words) - 16:02, 3 April 2024 |
 | X-linked spinal muscular atrophy Intellectual developmental disorder, autosomal dominant 64, 65, and 70 Intellectual disability, autosomal dominant 1 Intellectual... 14 KB (1,343 words) - 23:07, 26 April 2024 |
 | muscle hyperplasia, muscle hypertrophy, muscle pseudohypertrophy (muscle atrophy with infiltration of fat or other tissue), or symmetrical subcutaneous... 68 KB (3,992 words) - 06:52, 22 April 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) - 18:07, 28 February 2024 |
Lamellar recessive ichthyosis Landau–Kleffner syndrome Landouzy–Dejerine muscular dystrophy Landy–Donnai syndrome Langdon Down Langer–Nishino–Yamaguchi syndrome... 10 KB (900 words) - 15:15, 1 April 2022 |
Synthetase Mutations in Charcot-Marie-Tooth Disease Type 2D and Distal Spinal Muscular Atrophy Type V". The American Journal of Human Genetics. 72 (5):... 9 KB (907 words) - 03:13, 4 February 2024 |
Arthrogryposis renal dysfunction cholestasis syndrome Arthrogryposis spinal muscular atrophy Arylsulfatase A deficiency Asbestosis Ascariasis Ascher's syndrome... 23 KB (1,929 words) - 03:48, 26 April 2024 |