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What is another word for Congenital Myotonic Dystrophies?

Pronunciation: [kənd͡ʒˈɛnɪtə͡l mˌa͡ɪətˈɒnɪk dˈɪstɹəfɪz] (IPA)

Congenital Myotonic Dystrophies, also known as Congenital Myotonic Dystrophy (CMD), is a rare genetic disorder that affects muscles and various body systems from birth. CMD is characterized by muscle weakness, myotonia (prolonged muscle contraction), and delayed development. Synonyms for CMD include congenital muscular dystrophy type 1 (CMD1), Myotonic Dystrophy Type 1 (DM1), Steinert's disease, and dystrophia myotonica. Each of these terms refers to the same condition but may be used in different medical contexts or regions. It is important to recognize these synonyms in order to facilitate better communication, improve treatment approaches, and enhance awareness about this complex disorder among healthcare professionals and patients alike.
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What are the opposite words for Congenital Myotonic Dystrophies?

Antonyms for the term "Congenital Myotonic Dystrophies" would include "acquired," "adult-onset," and "non-hereditary." Unlike congenital myotonic dystrophies, these conditions develop over time, typically later in life. Acquired myotonic dystrophy can result from a variety of causes, such as exposure to certain medications or toxins. Adult-onset myotonic dystrophy typically appears in the patient's 20s or 30s, while non-hereditary forms may be caused by nerve damage or other factors. Although these conditions may share some symptoms with congenital myotonic dystrophies, they are fundamentally different in their causes, symptoms, and treatments.

What are the antonyms for Congenital myotonic dystrophies?

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