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What is another word for Dejerine Sottas Disease?

Pronunciation: [dɪd͡ʒˈɛɹiːn sˈɒtəz dɪzˈiːz] (IPA)

Dejerine Sottas Disease, also known as hereditary motor and sensory neuropathy type III, is a rare genetic disorder characterized by the degeneration of peripheral nerves. This condition typically manifests during infancy or early childhood, and its symptoms include muscle weakness, loss of sensation, and difficulty walking. Synonyms for Dejerine Sottas Disease can include hereditary motor and sensory neuropathy type III, HMSN type III, chronic hypertrophic neuropathy, and progressive hypertrophic neuropathy. These terms are used interchangeably to refer to the same medical condition, highlighting the various ways healthcare professionals may describe the disease. Awareness of these synonyms can aid in better understanding and communication between patients, caregivers, and medical professionals.
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What are the opposite words for Dejerine Sottas Disease?

Dejerine Sottas Disease is a rare genetic condition that affects the nerves of the body. The disease is often characterized by a progressive and severe loss of sensation and muscle strength in the limbs. While there are no direct antonyms for this disorder, some words that may be helpful in understanding the opposite of the symptoms of Dejerine Sottas Disease include improved sensation, strength, and coordination. Other terms that may be relevant include increased mobility, range of motion, and control over bodily movements. Ultimately, the goal of treatment for Dejerine Sottas Disease is to enhance these qualities and improve the overall quality of life for those affected by this condition.

What are the antonyms for Dejerine sottas disease?

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