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What is another word for Distal Spinal Muscular Atrophy?

Pronunciation: [dɪstˈal spˈa͡ɪnə͡l mˈʌskjʊləɹ ˈatɹəfi] (IPA)

Distal Spinal Muscular Atrophy, also known as spinal muscular atrophy type 1, is a genetic disorder that affects the muscles in the arms and legs. It is characterized by progressive muscle weakness and wasting, leading to difficulty in performing everyday tasks. Synonyms for this condition include distal spinal muscular dystrophy, spinal muscular atrophy type III, and childhood-onset distal SMA. These terms are used interchangeably to describe the same condition. While the names may differ slightly, they all refer to a neurodegenerative disorder that primarily affects the muscles in the distal regions of the body, leading to progressive muscle weakness and loss of motor function.
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What are the opposite words for Distal Spinal Muscular Atrophy?

Distal Spinal Muscular Atrophy (DSMA) is a genetic condition that affects the motor neurons of the spinal cord, leading to progressive muscle weakness and wasting. The disease has no antonyms, as it is a medical term that refers to a specific condition. However, the opposite of the symptoms associated with DSMA would be strength and vitality. Patients with DSMA often experience a loss of muscle control, so antonyms could include stability, coordination, and agility. Other antonyms that could be applied to DSMA include preservation, growth, and development, as the disease can impact a patient's ability to maintain muscle mass and grow stronger over time.

What are the antonyms for Distal spinal muscular atrophy?

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