Congenital muscular dystrophy symptoms
[DOCX File]Athena Diagnostics - Home - Advanced diagnostic testing ...
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Ulrich and merosin-deficient are two of the most common types of congenital muscular dystrophy. Myotonic dystrophy Symptoms, which are unpredictable and can occur at any age, may include muscle weakness in the face, jaw and neck, leading to speech and communication difficulties.
[DOCX File]Muscular Dystrophy UK
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Duchenne dystrophy, congenital muscular dystrophy, myotonic dystrophy, and facioscapulohumeral dystrophy are not included in this guideline, as they will be discussed in forthcoming guidelines. ... Clinicians should refer muscular dystrophy patients with signs or symptoms of cardiac failure for cardiology evaluation (e.g., medical management ...
[DOC File]Evidence-based Guideline: Diagnosis and Treatment of Limb ...
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The Muscular Dystrophy Community Assistance, Research, and Education Amendments of 2001 (MD-CARE Act; P.L. 107-84) authorized the establishment of the MDCC, with members appointed by the Secretary of the Department of Health and Human Services, in order to coordinate activities across the National Institutes of Health (NIH) and with other ...
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Congenital muscular dystrophy (CMD): a heterogeneous group of inherited muscular dystrophies that typically manifest with weakness apparent at birth or in early infancy. Infants may present with hypotonia or fail to meet motor milestones. It may overlap with LGMD or …
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