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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) (14.3%)
      
    • Becker Muscular Dystrophy (BMD) (7.1%)
      
    • Emery-Dreifuss Muscular Dystrophy (EDMD) (0%)
      
    • Limb-Girdle Muscular Dystrophy (LGMD) (14.3%)
      
    • Facioscapulohumeral Muscular Dystrophy (FSH or FSHD) (7.1%)
      
    • Myotonic Dystrophy (MMD) (7.1%)
      
    • Oculopharyngeal Muscular Dystrophy (OPMD) (0%)
      
    • Distal Muscular Dystrophy (DD) (Miyoshi) (0%)
      
    • Congenital Muscular Dystrophy (CMD) (3.6%)
      
    • Amyotrophic Lateral Sclerosis (ALS) (Also known as Lou Gehrig's Disease) (0%)
      
    • Spinal Muscular Atrophy Type 1 (SMA1, Werdnig-Hoffmann Disease) (3.6%)
      
    • Spinal Muscular Atrophy Type 2 (SMA2) (7.1%)
      
    • Spinal Muscular Atrophy Type 3 (SMA3, Kugelberg-Welander Disease) (7.1%)
      
    • 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) (7.1%)
      
    • 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) (3.6%)
      
    • Friedreich's Ataxia (FA) (0%)
      
    • Dejerine-Sottas Disease (DS) (chromosome 19 recessive form can be called CMT4F) (0%)
      
    • Dermatomyositis (DM) (0%)
      
    • Polymyositis (PM) (3.6%)
      
    • Inclusion Body Myositis (IBM) (3.6%)
      
    • 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) (3.6%)
      
    • 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. (7.1%)
      

    • Total Votes: 28

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