muscle spinal - significado y definición. Qué es muscle spinal
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Qué (quién) es muscle spinal - definición

GROUP OF DISEASES
Spinomuscular atrophy; Infantile Spinal Muscular Atrophy; Intermediate Spinal Muscular Atrophy; Spinal muscle atrophy; SMAs

Spinal muscular atrophies         
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. While some SMAs lead to early infant death, other diseases of this group permit normal adult life with only mild weakness.
Spinal anaesthesia         
  • Schematic drawing showing the principles of spinal anaesthesia.
FORM OF NEURAXIAL REGIONAL ANAESTHESIA
Spinal anesthesia; Spinal analgesia; Spinal block; Spinal needle; Spinal anesthetic; Spinal anaesthetic; Anesthesia, spinal; Intradural anesthesia
Spinal anaesthesia (or spinal anesthesia), also called spinal block, subarachnoid block, intradural block and intrathecal block, is a form of neuraxial regional anaesthesia involving the injection of a local anaesthetic or opioid into the subarachnoid space, generally through a fine needle, usually long. It is a safe and effective form of anesthesia usually performed by anesthesiologists that can be used as an alternative to general anesthesia commonly in surgeries involving the lower extremities and surgeries below the umbilicus.
Spinal manipulation         
ADJUSTMENT AND MANIPULATION OF THE VERTEBRAL COLUMN
Spinal manipulative therapy
Spinal manipulation is an intervention performed on spinal articulations, synovial joints, which is asserted to be therapeutic. These articulations in the spine that are amenable to spinal manipulative therapy include the z-joints, the atlanto-occipital, atlanto-axial, lumbosacral, sacroiliac, costotransverse and costovertebral joints.

Wikipedia

Spinal muscular atrophies

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. While some SMAs lead to early infant death, other diseases of this group permit normal adult life with only mild weakness.