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Spinal muscular atrophy (SMA) is a rare neuromuscular disorder that results in the loss of motor neurons and progressive muscle wasting. [3] [4] [5] It is usually diagnosed in infancy or early childhood and if left untreated it is the most common genetic cause of infant death. [6]
Bachelor of Science in Medical (Clinical) Laboratory Sciences (BSMT, BSMLS, BSCLS degrees, MLS Certification Eligible if from a NAACLS accredited program) Masters of Science in Medical (Clinical) Laboratory Sciences (MSMLS, MSCLS degrees) Doctor of Science in Clinical Laboratory Sciences (DSCLS degree)
SMA: sequential multiple analysis superior mesenteric artery spinal muscle atrophy SMA-6: six-channel serum multiple analysis SMA-7: serum metabolic assay SMN: statement of medical necessity SMS: senior medical student SMT: spinal manipulative therapy: SMV: superior mesenteric vein: SN: student nurse skilled nursing SNB: sentinel node biopsy ...
A medical degree is a professional degree admitted to those who have passed coursework in the fields of medicine and/or surgery from an accredited medical school.Obtaining a degree in medicine allows for the recipient to continue on into specialty training with the end goal of securing a license to practice within their respective jurisdiction.
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Spinal muscular atrophies (SMAs) are a genetically and clinically heterogeneous group of rare debilitating disorders characterised by the degeneration of lower motor neurons (neuronal cells situated in the anterior horn of the spinal cord) and subsequent atrophy (wasting) of various muscle groups in the body. [1]
The supplementary motor area (SMA) is a part of the motor cortex of primates that contributes to the control of movement. It is located on the midline surface of the hemisphere just in front of (anterior to) the primary motor cortex leg representation. In monkeys, the SMA contains a rough map of the body. In humans, the body map is not apparent.
SMA syndrome can present in two forms: chronic/congenital or acute/induced. [citation needed] Patients with the chronic, congenital form of SMA syndrome predominantly have a lengthy or even lifelong history of abdominal complaints with intermittent exacerbations depending on the degree of duodenal compression.