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830 Possible Causes for Circumoral Paresthesia, Facial Numbness, 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
  • Migraine

    A 45-year-old woman with a 20-year history of migrainous headaches presented with complaints of rightsided facial and hand numbness and paraesthesia.[ncbi.nlm.nih.gov] Patients may also experience nausea, vomiting, anorexia, neck pain, dizziness, changes in hearing, light sensitivity, difficulty concentrating, facial numbness or weakness[migrainepal.com]

    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
  • Hypocalcemia

    This is most commonly manifested as numbness and tingling, particularly of the distal extremities or as circumoral paresthesias.[endocrinologyadvisor.com] Symptoms include numbness and/or tingling of the hands, feet, or lips, muscle cramps, muscle spasms, seizures, facial twitching, muscle weakness, lightheadedness, and slow[medicinenet.com] […] of the fingertips and perioral area Chvostek's sign: Twitching of the ipsilateral facial musculature (perioral, nasal, and eye muscles) by tapping over cranial nerve VII[medicine.uiowa.edu]

    Missing: Mutation in the Tight Junction Protein 2 Gene
  • Basilar-Type 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
  • Metabolic Alkalosis

    paresthesia Muscle twitching, weakness Dizziness May exhibit: Hypertonicity of muscles, tetany, tremors, convulsions, loss of reflexes Confusion, irritability, restlessness[nurseslabs.com] numbness Reduced rate of respiration is one of the initial symptoms of this condition.[hxbenefit.com] […] intake; excessive ingestion of licorice Recurrent indigestion/heartburn with frequent use of antacids/baking soda NEUROSENSORY May report: Tingling of fingers and toes; circumoral[nurseslabs.com]

    Missing: Mutation in the Tight Junction Protein 2 Gene
  • Respiratory Alkalosis

    Acute respiratory alkalosis causes light-headedness, confusion, peripheral and circumoral paresthesias, cramps, and syncope.[msdmanuals.com] […] and peripheral paresthesias, carpopedal spasms, twitching and muscle weakness.[nurseslabs.com] […] limb paresthesias Cramps Tremor CNS Signs Ataxia Chvostek’s sign Tremor Encephalopathy Coma Seizure manifestations PNS Signs Myoclonus Tetany I have written about these[leonchaitow.com]

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

    2015 ICD-9-CM Diagnosis Code 276.3 Alkalosis 2015 Billable Thru Sept 30/2015 Non-Billable On/After Oct 1/2015 ICD-9-CM 276.3 is a billable medical code that can be used to indicate a diagnosis on a reimbursement claim, however, 276.3 should only be used for claims with a date of service on or before September 30, 2015.[…][icd9data.com]

    Missing: Mutation in the Tight Junction Protein 2 Gene