Results 1 - 5 of 5 for dermatomyositis OR "telangiectasia," hereditary benign
  1. Arteriovenous Malformations and Other Vascular Lesions of the Central Nervous System From the National Institutes of Health (National Institute of Neurological Disorders and Stroke)  
    ... medical syndromes known to be hereditary. They include hereditary hemorrhagic telangiectasia (also known as Osler-Weber-Rendu disease ), Sturge- ... genetic basis of familial cavernous malformations and other hereditary ... telangiectasia. Other scientists are seeking to refine the techniques ...
  2. Rare Diseases Clinical Research Network (Rare Diseases Clinical Research Network)  
    ... Brain Vascular Malformation Consortium Familial Cavernous Malformations (CCM) Hereditary Hemorrhagic Telangiectasia (HHT) Brain Arteriovenous Malformation (BAVM) Sturge-Weber Syndrome ( ...
  3. Rare Diseases and Related Terms From the National Institutes of Health (Office of Rare Diseases)  
    ... dominant form of benign neonatal seizures - See Convulsions benign familial neonatal dominant form * Autosomal dominant hereditary demyelinating motor and sensory neuropathy - See Charcot-Marie- ...
  4. National Institute of Neurological Disorders and Stroke (National Institute of Neurological Disorders and Stroke)  
    ... Chiari Malformation Arteriovenous Malformation Aspartame Asperger ... Essential Blepharospasm Benign Focal Amyotrophy Benign Intracranial Hypertension ...
  5. ... 7, a protein that participates in muscle contraction. Hereditary inclusion-body myositis (myopathy) type 1 (HIBM1) HIBM1 ... bulbar muscular atrophy ( Kennedy disease) Inflammatory Myopathies Polymyositis Dermatomyositis Inclusion-body myositis Diseases of Neuromuscular Junction Myasthenia ...
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