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3,113 Possible Causes for Cyanosis, EMG Shows Neurogenic Abnormalities, Facial Muscle Weakness and Progressive Atrophy

  • Spinal Muscular Atrophy Type 1

    We present a baby with spinal muscular atrophy type 1, an inherited disorder causing progressive weakness, leading to complete paralysis of respiratory, facial and limb muscles[ncbi.nlm.nih.gov] Spinal muscular atrophy is characterised by slowly progressive muscle weakness and atrophy of the limb muscles associated with motor neurone loss in the spinal cord.[patient.info] Bulbar muscular atrophy affects the bulbar and facial muscles with motor neurone loss in the brainstem. [ 1 ] The spinal muscular atrophies (SMAs) are a spectrum of genetically[patient.info]

  • Distal Spinal Muscular Atrophy Type 3

    At 6 months, he had acute onset respiratory distress and cyanosis requiring intubation and ventilation.[annalsofian.org] Spinal muscular atrophy is characterised by slowly progressive muscle weakness and atrophy of the limb muscles associated with motor neurone loss in the spinal cord.[patient.info] Prolonged cyanosis may be noted at delivery. In some instances, the disease can cause fulminant weakness in the first few days of life.[slideshare.net]

  • Spinal Muscular Atrophy Type 4

    Prolonged cyanosis may be noted at delivery. In some instances, the disease can cause fulminant weakness in the first few days of life.[emedicine.medscape.com] Spinal muscular atrophy is characterised by slowly progressive muscle weakness and atrophy of the limb muscles associated with motor neurone loss in the spinal cord.[patient.info] Scapuloperoneal spinal muscular atrophy: Type 1 (AD form) appears at age 14-26, with weakness, distal leg atrophy, and absent tendon reflexes and sparing of intrinsic foot[emedicine.medscape.com]

  • Spinal Muscular Atrophy

    Spinal muscular atrophy is characterised by slowly progressive muscle weakness and atrophy of the limb muscles associated with motor neurone loss in the spinal cord.[patient.info] Bulbar muscular atrophy affects the bulbar and facial muscles with motor neurone loss in the brainstem. [ 1 ] The spinal muscular atrophies (SMAs) are a spectrum of genetically[patient.info] They all result in progressive lower motor neurone weakness. The gene defect is on chromosome 5q and the implicated gene is called survival motor neurone gene 1 (SMN1).[patient.info]

    Missing: EMG Shows Neurogenic Abnormalities
  • Spinal Muscular Atrophy Type 2

    Spinal muscular atrophy is characterised by slowly progressive muscle weakness and atrophy of the limb muscles associated with motor neurone loss in the spinal cord.[patient.info] Bulbar muscular atrophy affects the bulbar and facial muscles with motor neurone loss in the brainstem. [ 1 ] The spinal muscular atrophies (SMAs) are a spectrum of genetically[patient.info] They all result in progressive lower motor neurone weakness. The gene defect is on chromosome 5q and the implicated gene is called survival motor neurone gene 1 (SMN1).[patient.info]

    Missing: Cyanosis
  • Raynaud Phenomenon

    These can either be triphasic (pallor, cyanosis, and hyperemia), biphasic (cyanosis and erythema), or uni-phasic (either pallor or cyanosis) in nature.[symptoma.com] Methemoglobinemia and sulfhemoglobinemia are rare causes of cyanosis that can be medication-induced. Both are known complications of therapy with phenazopyridine.[ncbi.nlm.nih.gov] Signs Pallor or Cyanosis of fingers or toes Thumb is not involved VIII.[fpnotebook.com]

    Missing: EMG Shows Neurogenic Abnormalities Facial Muscle Weakness and Progressive Atrophy
  • Raynaud's Disease

    In some patients only pallor or cyanosis occurs.[jamanetwork.com] Attacks were defined as occurring if two of the possible three color changes (pallor, cyanosis, and rubor) occurred, and serial photographs were scored by three independent[ncbi.nlm.nih.gov] INTRODUCTION: Raynaud's disease is a disorder that is characterized by attacks of pain, cyanosis, redness, and numbness in the upper extremities caused by vasospasm of digital[ncbi.nlm.nih.gov]

    Missing: EMG Shows Neurogenic Abnormalities Facial Muscle Weakness and Progressive Atrophy
  • Cold Exposure

    INTRODUCTION: Exposure to cold temperature is a serious but often neglected problem in prehospital care. It not only is an uncomfortable, subjective experience, but it also can cause severe disturbances in vital functions, gradually leading to hypothermia. OBJECTIVE: The aim of this study was to examine healthy[…][ncbi.nlm.nih.gov]

    Missing: EMG Shows Neurogenic Abnormalities Facial Muscle Weakness and Progressive Atrophy
  • Atelectasis

    Atelectasis and Pneumothorax Lungs Pain Trouble breathing Faintness Cyanosis Mucus plug Tumor Inhaled foreign object Physical trauma to the lung Wound Overview Atelectasis[nm.org] Symptoms In acute atelectasis in which there is sudden obstruction of the bronchus, there may be dyspnea and cyanosis, elevation of temperature, a drop in blood pressure,[healthcentral.com] The heart rate and breathing rate may increase, and sometimes the person may look bluish (a condition called cyanosis ) because oxygen levels in the blood are low.[merck.com]

    Missing: EMG Shows Neurogenic Abnormalities Facial Muscle Weakness and Progressive Atrophy
  • Asthma

    […] you: otc inhalers Seek medical help immediately for: Fast breathing with chest retractions (skin sucks in between or around the chest plate and/or rib bones when inhaling) Cyanosis[aafa.org] Extrathoracic respiratory signs should also be systematically looked for, including cyanosis, finger deformation, pulsus paradoxus, and pursed lips breathing.[erj.ersjournals.com] Advanced COPD symptoms include cyanosis, headaches, weight loss, pulmonary hypertension, and coughing up blood. What is COPD?[web.archive.org]

    Missing: EMG Shows Neurogenic Abnormalities Facial Muscle Weakness and Progressive Atrophy

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