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[POLL]: What type of Muscular Dystrophy do you have?

Last post Tue, Mar 25 2008 12:39 PM by brokenwings. 0 replies.

• brokenwings

  Posts: 73

  • [POLL]: What type of Muscular Dystrophy...
  • Posted: Tue, Mar 25 2008 12:39 PM

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  • Hey, here is a poll so we can see how many people are dealing with what types of MD at a glance here. :) 

    What type of Muscular Dystrophy do you have?

    
    

    • Duchenne Muscular Dystrophy (DMD) (14.8%)
      
    • Becker Muscular Dystrophy (BMD) (7.4%)
      
    • Emery-Dreifuss Muscular Dystrophy (EDMD) (0%)
      
    • Limb-Girdle Muscular Dystrophy (LGMD) (14.8%)
      
    • Facioscapulohumeral Muscular Dystrophy (FSH or FSHD) (7.4%)
      
    • Myotonic Dystrophy (MMD) (7.4%)
      
    • Oculopharyngeal Muscular Dystrophy (OPMD) (0%)
      
    • Distal Muscular Dystrophy (DD) (Miyoshi) (0%)
      
    • Congenital Muscular Dystrophy (CMD) (3.7%)
      
    • Amyotrophic Lateral Sclerosis (ALS) (Also known as Lou Gehrig's Disease) (0%)
      
    • Spinal Muscular Atrophy Type 1 (SMA1, Werdnig-Hoffmann Disease) (3.7%)
      
    • Spinal Muscular Atrophy Type 2 (SMA2) (7.4%)
      
    • Spinal Muscular Atrophy Type 3 (SMA3, Kugelberg-Welander Disease) (7.4%)
      
    • Spinal Bulbar Muscular Atrophy (SBMA) (Also known as Kennedy Disease and X-Linked SBMA) (0%)
      
    • Phosphorylase Deficiency (MPD or PYGM) (Also known as McArdle Disease) (0%)
      
    • Acid Maltase Deficiency (AMD) (Also known as Pompe Disease) (0%)
      
    • Phosphofructokinase Deficiency (Also known as Tarui Disease) (0%)
      
    • Debrancher Enzyme Deficiency (DBD) (Also known as Cori or Forbes Disease) (0%)
      
    • Mitochondrial Myopathy (MITO) (7.4%)
      
    • Carnitine Deficiency (CD) (0%)
      
    • Carnitine Palmityl Transferase Deficiency (CPT) (0%)
      
    • Phosphoglycerate Kinase Deficiency (0%)
      
    • Phosphoglycerate Mutase Deficiency (0%)
      
    • Lactate Dehydrogenase Deficiency (0%)
      
    • Myoadenylate Deaminase Deficiency (0%)
      
    • Mitochondrial Disease- Other (0%)
      
    • Charcot-Marie-Tooth Disease (CMT) (Also known as Hereditary Motor and Sensory Neuropathy (HMSN) or Peroneal Muscular Atrophy (PMA) (3.7%)
      
    • Friedreich's Ataxia (FA) (0%)
      
    • Dejerine-Sottas Disease (DS) (chromosome 19 recessive form can be called CMT4F) (0%)
      
    • Dermatomyositis (DM) (0%)
      
    • Polymyositis (PM) (3.7%)
      
    • Inclusion Body Myositis (IBM) (3.7%)
      
    • Myasthenia Gravis (MG) (0%)
      
    • Lambert-Eaton Syndrome (LES) (0%)
      
    • Congenital Myasthenic Syndrome (CMS) (0%)
      
    • Hyperthyroid Myopathy (HYPTM) (0%)
      
    • Hypothyroid Myopathy (HYPOTM) (0%)
      
    • Myotonia Congenita (MC) (Two forms: Thomsen and Becker Disease) (0%)
      
    • Paramyotonia Congenita (PC) (0%)
      
    • Central Core Disease (CCD) (0%)
      
    • Nemaline Myopathy (NM) (0%)
      
    • Myotubular Myopathy/Centronuclear Myopathy (MTM or CNM) (0%)
      
    • Periodic Paralysis (PP) (Two forms: Hypokalemic and Hyperkalemic) (0%)
      
    • Muscular Dystrophy- Unspecified (0%)
      
    • Muscular Dystrophy/Myopathy- Other (0%)
      
    • I do not have Muscular Dystrophy. (7.4%)
      

    • Total Votes: 27

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  Filed under: Lou Gehrig's Disease, Kugelberg-Welander Disease, Lactate Dehydrogenase Deficiency, Amyotrophic Lateral Sclerosis, Becker Disease, Becker Muscular dystrophy, Forbes Disease, Cori, mito, mitochondrial disease, Mitochondrial Myopathy, Miyoshi, metabolic disease of the muscle, Dejerine-Sottas Disease, Hyperkalemic, Hyperthyroid Myopathy, Hypokalemic, Hypothyroid Myopathy, Phosphofructokinase Deficiency, Phosphoglycerate Kinase Deficiency, Phosphoglycerate Mutase Deficiency, Phosphorylase Deficiency, Thomsen, Pseudohypertrophic, poll, Polymyositis, Pompe Disease, Debrancher Enzyme Deficiency, Nemaline Myopathy, X-Linked SBMA, Oculopharyngeal Muscular Dystrophy, Dermatomyositis, Tarui Disease, Paramyotonia Congenita, ALS, Central Core Disease, Centronuclear Myopathy, Werdnig-Hoffmann Disease, McArdle Disease, MDA, Myasthenia Gravis, Myoadenylate Deaminase Deficiency, myopathy, Myotonia Congenita, Myotonic Dystrophy, Myotubular Myopathy, Distal Muscular Dystrophy, Limb-Girdle Muscular Dystrophy, Steinert Disease, Spinal Muscular Atrophy Type 1, Spinal Muscular Atrophy Type 2, Spinal Muscular Atrophy Type 3, Lambert-Eaton Syndrome, Landouzy-Dejerine, Emery-Dreifuss Muscular Dystrophy, Duchenne Muscular Dystrophy, Kennedy Disease, Hereditary Motor and Sensory Neuropathy, Acid Maltase Deficiency, Carnitine Deficiency, Carnitine Palmityl Transferase Deficiency, Charcot-Marie-Tooth Disease, Periodic Paralysis, Peroneal Muscular Atrophy, Friedreich's Ataxia, Spinal Bulbar Muscular Atrophy, muscle biopsies, Muscular Dystrophy, Congenital Muscular Dystrophy, Congenital Myasthenic Syndrome, Inclusion Body Myositis, Facioscapulohumeral Muscular Dystrophy
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