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What is another word for Childhood Onset Nemaline Myopathy?

Pronunciation: [t͡ʃˈa͡ɪldhʊd ˈɒnsɛt nˈɛməlˌa͡ɪn ma͡ɪˈɒpəθɪ] (IPA)

Childhood Onset Nemaline Myopathy (CONM) is a rare genetic disorder that affects muscle strength and tone. Also known as nemaline myopathy, this condition primarily emerges during childhood and manifests through muscle weakness, delayed motor skills, and respiratory difficulties. This hereditary condition is caused by mutations in the nebulin (NEB) gene, which is responsible for muscle development and function. While there currently aren't many synonyms for Childhood Onset Nemaline Myopathy, it is sometimes referred to as nemaline rod myopathy, rod body myopathy, or congenital nemaline myopathy. Timely diagnosis and proper management are crucial to enhance the quality of life for individuals living with CONM.
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What are the opposite words for Childhood Onset Nemaline Myopathy?

Antonyms for Childhood Onset Nemaline Myopathy (CNM) may include terms such as healthy, able-bodied or normal muscle function. CNM is a rare, genetic neuromuscular disorder that can lead to muscle weakness, breathing difficulties and decreased mobility. Antonyms for CNM represent the opposite effect of the condition and describe individuals who have normal muscle function and are free from the symptoms associated with CNM. Such individuals are able to lead an active and independent lifestyle, without the need for medical assistance. Early detection and management are important for those affected by childhood onset nemaline myopathy, and medical intervention can help manage the symptoms of the condition.

What are the antonyms for Childhood onset nemaline myopathy?

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