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Emery Dreyfuss muscular dystrophy X linked (XL-EDMD) OMIT 310300 Gene: Emerging Locus: Xq28 SERVICE: mutation analysis of the emerging gene TESTING: Diagnostic: Carrier: Prenatal: OMIT: 300384 clinically
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What is emery dreifuss muscular dystrophy?
Emery-Dreifuss muscular dystrophy is a rare form of muscular dystrophy that primarily affects muscles used for movement (skeletal muscles) and the heart.
Who is required to file emery dreifuss muscular dystrophy?
Healthcare providers and researchers studying muscular dystrophy may be required to report cases of Emery-Dreifuss muscular dystrophy.
How to fill out emery dreifuss muscular dystrophy?
The reporting requirements for Emery-Dreifuss muscular dystrophy may vary by jurisdiction, but typically involve providing detailed information about the patient's medical history, symptoms, and diagnosis.
What is the purpose of emery dreifuss muscular dystrophy?
The purpose of reporting cases of Emery-Dreifuss muscular dystrophy is to better understand the prevalence and characteristics of this rare condition, and to improve diagnosis and treatment options for affected individuals.
What information must be reported on emery dreifuss muscular dystrophy?
Information reported on Emery-Dreifuss muscular dystrophy may include patient demographics, genetic testing results, symptoms, and progression of the disease.
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