Article

Differential Diagnostic Decision-Making Scheme for Limb Weakness and Bilateral Temporal Pole Abnormal Signals

2026-02-03

Abstract excerpt

<title>Abstract</title> <p> <bold>Background</bold> : Myotonic dystrophy type 1 (DM1) is an autosomal dominant disorder caused by an abnormal expansion of the CTG trinucleotide repeat in the 3′UTR region of the DMPK gene on chromosome 19q13.3. There is currently no cure for DM1, and early diagnosis along with multidisciplinary evaluation and intervention may be important in delaying its progression. However, it...

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Literature Corpus work: a322c7bb-aed8-562a-b795-d8b25d71d0da
DOI: 10.21203/rs.3.rs-8370605/v1

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