| PSMA | proximal spinal muscular atrophy |
|---|---|
| SBMA | spinal bulbar muscular atrophy |
| SMA | sequential multiple analysis or analyzer; sequential multichannel autoanalyzer; simultaneous multich... |
| SPMA | spinal progressive muscular atrophy |
| PMD | Progressive Muscular Dystrophy; 진행성 근이영양증 Types of PMD(Progressive Muscular Dystroph... |
| juvenile muscular atrophy | Slowly progressive proximal muscular weakness and wasting, beginning in childhood, caused by degeneration of motor neurons in the anterior horns of the spinal cord; onset usually between 2 and 17 years of age; usually autosomal recessive inheritance. Synonym: juvenile muscular atrophy, Kugelberg-Welander disease, Wohlfart-Kugelberg-Welander disease. (05 Mar 2000) |
|---|---|
| juvenile spinal muscular atrophy | Slowly progressive proximal muscular weakness and wasting, beginning in childhood, caused by degeneration of motor neurons in the anterior horns of the spinal cord; onset usually between 2 and 17 years of age; usually autosomal recessive inheritance. Synonym: juvenile muscular atrophy, Kugelberg-Welander disease, Wohlfart-Kugelberg-Welander disease. (05 Mar 2000) |
| familial spinal muscular atrophy | Transmitted as autosomal recessive on chromosome 5q. Progressive dysfunction of the anterior horn cells in the spinal cord and brainstem cranial nerves with profound weakness and bulbar dysfunction occurring in the first two years of life. Three groups, based on age of clinical onset, are recognised. Synonym: familial spinal muscular atrophy, Hoffmann's muscular atrophy, infantile muscular atrophy, infantile progressive spinal muscular atrophy, progressive infantile spinal muscular atrophy, Werdnig-Hoffmann disease, Werdnig-Hoffmann muscular atrophy. (05 Mar 2000) |
| arthropathy, neurogenic | Chronic progressive degeneration of the stress-bearing portion of a joint, with bizarre hypertrophic changes at the periphery. It is probably a complication of a variety of neurologic disorders, particularly tabes dorsalis, involving loss of sensation, which leads to relaxation of supporting structures and chronic instability of the joint. (12 Dec 1998) |
| autonomic neurogenic bladder | Malfunctioning bladder, secondary to low spinal cord lesions. (05 Mar 2000) |
| bladder, neurogenic | Any condition of dysfunction of the urinary bladder caused by a lesion of the central or peripheral nervous system. (12 Dec 1998) |
| reflex neurogenic bladder | An abnormal condition of bladder function whereby the bladder is cut off from upper motor neuron control, but where the lower motor neuron arc is still intact. (05 Mar 2000) |
| neurogenic | <embryology> Arising from or caused by the nervous system. Origin: Gr. Gennan = to produce (27 Sep 1997) |
| neurogenic bladder | A dysfunction of the bladder due a malfunction of the autonomic nerves which control bladder function. (27 Sep 1997) |
| neurogenic fracture | A fracture in bone weakened by disease of the nerve supply. (05 Mar 2000) |
| neurogenic gene | Best described in Drosophila, genes that are required to determine a neuronal fate. Examples: Notch, Delta. (18 Nov 1997) |
| neurogenic shock | <neurology> This form of distributive shock results from a change in systemic vascular resistance, mediated by a neurologic injury (for example, head injury, spinal cord injury). Synonym: spinal shock. (27 Sep 1997) |
| neurogenic tonus | Contraction of a muscle caused by the influence of its extrinsic nerve supply (05 Mar 2000) |
| nonneurogenic neurogenic bladder | <urology> Detrusor-sphincter incoordination with urinary incontinence, constipation, urinary tract infection, upper tract changes. Synonym: Hinman syndrome, pseudoneurogenic bladder. (05 Mar 2000) |
| disputed neurogenic thoracic outlet syndrome | <syndrome> A highly controversial disorder in which the brachial plexus is reputedly repressed at one or more sites along its course, particularly within the interscalene triangle, and between the normal first thoracic rib and some other structures; frequently attributed to trauma (particularly automobile accidents, and most often diagnosed in young to middle-aged women; no characteristic clinical presentation, although forequarter pain is characteristic; no definite objective findings are present, and no undisputed ancillary diagnostic studies are available. (05 Mar 2000) |