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5,091 Possible Causes for Hyperactive Brainstem Reflexes, Increased Serum Creatine Phosphate, Rapid Progression

  • Limb-Girdle Muscular Dystrophy Type 2C

    Progression is rapid, and patients are usually wheelchair-bound in adolescence.[sema4genomics.com] DMD is the most severe form of muscular dystrophy and it is characterized as follows1: Rapid progression of muscle weakness, often with calf hypertrophy Decreased levels of[centogene.com] The more common LGMD2 generally has an earlier age of onset, worse symptoms and more rapid progression compared to LGMD1.[chs-journal.com]

    Missing: Hyperactive Brainstem Reflexes
  • Autosomal Recessive Parkinson Disease 14

    […] disease progression.[acnr.co.uk] The disorder is characterized by progressive involuntary, rapid, jerky motions and mental deterioration.[encyclopedia.com] Patients with late forms of the disease associated with rapid progression, weight loss and respiratory failure should prompt screening of the DCTN1 gene associated with Perry[acnr.co.uk]

    Missing: Hyperactive Brainstem Reflexes
  • Spinal and Bulbar Muscular Atrophy

    progression leading to compromised ambulation in the mid-20s.[ncbi.nlm.nih.gov] […] tendon reflexes, and Babinski signs.[neuropathology-web.org] As with other trinucleotide repeat disorders, anticipation is frequently observed and larger CAG expansions are associated with earlier onset and a more rapid clinical progression[mayomedicallaboratories.com]

  • Limb-Girdle Muscular Dystrophy Type 2Q

    One family has shown rapid progression of the disorder in adolescence (summary by Gundesli et al., 2010).[ncbi.nlm.nih.gov] DMD is the most severe form of muscular dystrophy and it is characterized as follows1: Rapid progression of muscle weakness, often with calf hypertrophy Decreased levels of[centogene.com] The more common LGMD2 generally has an earlier age of onset, worse symptoms and more rapid progression compared to LGMD1.[chs-journal.com]

    Missing: Hyperactive Brainstem Reflexes
  • Danon Disease

    progression to heart failure.[ncbi.nlm.nih.gov] Heart transplantation is the reliable treatment once the occurrence of heart failure and should be considered as early as possible due to its rapid progression.[ncbi.nlm.nih.gov] CONCLUSION: We highlight the aggressive cardiac phenotype of Danon disease in our clinical experience with rapid progression to end-stage cardiomyopathy; this progression[ncbi.nlm.nih.gov]

    Missing: Hyperactive Brainstem Reflexes
  • Muscular Dystrophy-Dystroglycanopathy Type C14

    DMD is the most severe form of muscular dystrophy and it is characterized as follows1: Rapid progression of muscle weakness, often with calf hypertrophy Decreased levels of[centogene.com] The more common LGMD2 generally has an earlier age of onset, worse symptoms and more rapid progression compared to LGMD1.[chs-journal.com] Progression is rapid, and patients are usually wheelchair-bound in adolescence.[sema4genomics.com]

    Missing: Hyperactive Brainstem Reflexes
  • Limb-Girdle Muscular Dystrophy Type 2B

    progression, with or without pain [ 5 ].[ped-rheum.biomedcentral.com] DMD is the most severe form of muscular dystrophy and it is characterized as follows1: Rapid progression of muscle weakness, often with calf hypertrophy Decreased levels of[centogene.com] The more common LGMD2 generally has an earlier age of onset, worse symptoms and more rapid progression compared to LGMD1.[chs-journal.com]

    Missing: Hyperactive Brainstem Reflexes
  • Duchenne Muscular Dystrophy

    Duchenne muscular dystrophy is a severe recessive X-linked form of muscular dystrophy characterized by rapid progression of muscle degeneration.[disabled-world.com] Olson also said that progress would be rapid. “To launch a clinical trial, we need to scale up, improve efficiency and assess safety,” Dr. Olson said.[web.archive.org] Duchenne muscular dystrophy is a severe recessive X-linked form of muscular dystrophy characterized by rapid progression of muscle degeneration, eventually leading to pain[disabled-world.com]

    Missing: Hyperactive Brainstem Reflexes
  • Glycogen Storage Disease Type 2

    There is often a rapid progression to cardiac failure and death typically occurs within the first year.[genedx.com] Infantile-onset Pompe disease is associated with a rapid progression of disease severity and a high mortality rate. 3 Late-onset Pompe disease typically affects patients greater[avrobio.com] Its severity is quite variable, however, generally, the earlier the symptoms present, the more rapid progression.[mda.org.au]

    Missing: Hyperactive Brainstem Reflexes
  • Muscular Dystrophy-Dystroglycanopathy Type C9

    DMD is the most severe form of muscular dystrophy and it is characterized as follows1: Rapid progression of muscle weakness, often with calf hypertrophy Decreased levels of[centogene.com] The more common LGMD2 generally has an earlier age of onset, worse symptoms and more rapid progression compared to LGMD1.[chs-journal.com] Progression is rapid, and patients usually lose the ability to walk independently in adolescence.[sema4genomics.com]

    Missing: Hyperactive Brainstem Reflexes

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