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71 Possible Causes for Circumoral Paresthesia, Mutation in the Tight Junction Protein 2 Gene

  • Hyperventilation

    THE hyperventilation syndrome, as seen in anxious, tense persons, is characterized by paresthesia of the extremities and circumoral area, sensations of lightheadedness and[nejm.org]

    Missing: Mutation in the Tight Junction Protein 2 Gene
  • Hypomagnesemia

    It has been recently attributed to a mutation in the Claudin 16 (CLDN 16) gene of the Paracellin-1 (PCLN-1) tight junction protein.[ncbi.nlm.nih.gov] Herein, we report 2 sisters with FHHNC. Both sisters presented at an early stage with hypomagnesemia and hypocalcemia.[ncbi.nlm.nih.gov]

  • Acute Hyperventilation

    Abstract In 27 comatose patients with acute head injury, 45 paired studies of regional cerebral blood flow (rCBF) were performed before and after hyperventilation. In total 676 regions were studied, and rCBF was calculated as initial slope index using the intracarotid washout technique of 133 Xe. The tests were[…][ncbi.nlm.nih.gov]

    Missing: Mutation in the Tight Junction Protein 2 Gene
  • Panic Attacks

    The author gives an account of the analysis of a young woman suffering from severe panic attacks. He describes the initial problems of the setting and how they are progressively overcome, the emergence of highly structured psychotic nuclei and the gradual approach to the patient's splits. Whereas the panic[…][ncbi.nlm.nih.gov]

    Missing: Mutation in the Tight Junction Protein 2 Gene
  • Psychogenic Hyperventilation

    STUDY OBJECTIVE: Elevated arterial lactate levels are closely related to morbidity and mortality in various patient categories. In the present retrospective study, the relation between arterial lactate, partial pressure of carbon dioxide (Pco(2)) and pH was systematically investigated in patients who visited the[…][ncbi.nlm.nih.gov]

    Missing: Mutation in the Tight Junction Protein 2 Gene
  • Migraine

    Neurology. 2012 Apr 24; 78(17): 1337–1345. Report of the Quality Standards Subcommittee of the American Academy of Neurology and the American Headache Society S.D. Silberstein, MD, FACP, S. Holland, PhD, F. Freitag, DO, D.W. Dodick, MD, C. Argoff, MD, and E. Ashman, MD This article has been cited by other articles in[…][ncbi.nlm.nih.gov]

    Missing: Mutation in the Tight Junction Protein 2 Gene
  • Basilar Migraine

    BACKGROUND: It remains uncertain whether basilar-type migraine (BM) is a subtype of migraine with typical aura (MTA) or a distinct phenotype or genotype. OBJECTIVE: To analyze the symptomatology, familial distribution, and genotype of BM. METHODS: The authors recruited 105 families comprising 362 patients with MTA[…][ncbi.nlm.nih.gov]

    Missing: Mutation in the Tight Junction Protein 2 Gene
  • Hypocalcemia

    This is most commonly manifested as numbness and tingling, particularly of the distal extremities or as circumoral paresthesias.[endocrinologyadvisor.com]

    Missing: Mutation in the Tight Junction Protein 2 Gene
  • Malignant Neoplasm of Pancreas

    Pancreatic cancer is a type of cancer that starts in the pancreas. (Cancer starts when cells in the body begin to grow out of control. To learn more about how cancers start and spread, see What Is Cancer? ) Pancreatic adenocarcinoma is the most common type of pancreatic cancer. Pancreatic neuroendocrine[…][cancer.org]

    Missing: Mutation in the Tight Junction Protein 2 Gene
  • Systemic Scleroderma

    Systemic Scleroderma (SSc) is an autoimmune disease that affects connective tissue, resulting in hardening skin, reduced vascular perfusion, gingival fibrosis, enlarged periodontal ligament, xerostomia, and trigeminal neuralgia. Secondary effects, including reduced oral opening and reduced manual dexterity may[…][ncbi.nlm.nih.gov]

    Missing: Mutation in the Tight Junction Protein 2 Gene

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