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- in the realm of neuromuscular disease. Neuromuscular disorders do not only affect the neurological system. Many neuromuscular disorders can affect other8 KB (976 words) - 20:31, 27 November 2023
- Neuromuscular Disorders Overview/Members
- Proximal Weakness (category Muscle Disorders)pelvic girdle muscle weakness particularly in those with certain neuromuscular disorders. Gower thought it was pathognomonic for what is now called Duchenne6 KB (636 words) - 15:34, 11 March 2023
- McArdle Disease (category Muscle Disorders)571 KB (f) OMIM - McArdle Disease GeneReviews - McArdle Disease Neuromuscular Disorders - Amato 2008 Literature Review Reviews from the last 7 years: review4 KB (626 words) - 18:13, 12 March 2023
- Bowel Disease, Sarcoidosis Genetic: Heritable Connective Tissue Disorders, Neuromuscular Diseases (e.g. Myotonic Dystrophy type 2, Pompe Disease) Idiopathic:85 bytes (126 words) - 22:14, 23 March 2022
- the deformity and may eliminate it. Dynamic winging is due to a neuromuscular disorder, is visible with active and resisted movements, and is absent at5 KB (498 words) - 20:34, 11 March 2023
- Myotonic Dystrophy (category Muscle Disorders)dystrophy type 2 in patients with suspected fibromyalgia syndrome". Neuromuscular disorders: NMD. 26 (6): 370โ373. doi:10.1016/j.nmd.2016.03.009. ISSNย 1873-236411 KB (1,351 words) - 18:09, 12 March 2023
File:Mcdonald2012 neuromuscular disorders.pdf File uploaded with MsUpload(1.32 MB) - 13:37, 4 April 2021- Causes wasting, decreased tone, impaired or absent reflexes Neuromuscular junction disorders: Causes fatigable weakness, normal or decreased tone, normal15 KB (1,556 words) - 20:37, 11 March 2023
- Bowel Disease, Sarcoidosis Genetic: Heritable Connective Tissue Disorders, Neuromuscular Diseases (e.g. Myotonic Dystrophy type 2, Pompe Disease) Idiopathic:24 KB (3,236 words) - 18:38, 12 March 2023
- Ehlers Danlos Syndrome (category Heritable Connective Tissue Disorders)syndromes (EDS) are a heterogenous group of hereditary connective tissue disorders. The predominant features are joint hypermobility, abnormal skin texture26 KB (1,610 words) - 19:25, 16 December 2022
- Idiopathic Scoliosis (category Developmental Disorders)of cases. It is a diagnosis of exclusion and is differentiated from neuromuscular and congenital scoliosis. In adults degenerative scoliosis is a consideration31 KB (3,895 words) - 19:29, 11 November 2023
- involvement of the hands, legs, arms, face, and/or ears. Paroxysmal Extreme Pain Disorder typically begins during infancy or the neonatal period and includes autonomic8 KB (601 words) - 20:13, 19 May 2023
- 2004. CD003470. PMID: 15266488. DOI. Full Text. Martimbianco et al.. Neuromuscular electrical stimulation (NMES) for patellofemoral pain syndrome. The Cochrane3 KB (654 words) - 22:06, 17 April 2022
- Causes wasting, decreased tone, impaired or absent reflexes Neuromuscular junction disorders: Causes fatigable weakness, normal or decreased tone, normal15 KB (1,990 words) - 09:48, 12 March 2023
- Maps Thoracic Pain Maps Bone and Cartilage Disorders Select [โบ] to view subcategories Bone and Cartilage Disorders Fractures Osteoarthritis Bone Lesions Bone5 KB (863 words) - 18:15, 12 March 2023
- control. Additionally, deficits in proprioception can delay protective neuromuscular reflexes, leading to potential joint damage and abnormal movement patterns2 KB (313 words) - 19:30, 28 October 2023
- Bowel Disease, Sarcoidosis Genetic: Heritable Connective Tissue Disorders, Neuromuscular Diseases (e.g. Myotonic Dystrophy type 2, Pompe Disease) Idiopathic:20 KB (3,209 words) - 20:47, 22 February 2023
- organs; and the ฮฑ motor neurons. Characteristics of sensory nerve fibres Disorders known to contribute to SFN are listed below. SFN is a generalised sensory29 KB (3,612 words) - 21:12, 20 May 2023
- Muscle Cramps and Contractures (category Muscle Disorders)inherited causes. They are infrequently due to progressive systemic or neuromuscular diseases. Contractures are defined as muscle shortening resulting in5 KB (189 words) - 17:09, 21 March 2023