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797 Possible Causes for Facial Numbness, Focal Polymorphic Delta Slowing, Mutation in the Tight Junction Protein 2 Gene

  • Stroke

    A 48-year-old man presented with acute onset of left facial numbness, ataxic gait and double vision.[ncbi.nlm.nih.gov] In some cases, focal slow activity may presents as focal and irregular slow activity in the delta frequency, receiving the designation of polymorphic delta activity (PDA)[scielo.br] The symptoms may be mild or dramatic and can mimic a stroke with weakness, numbness, facial droop, and speech difficulties, but these symptoms may only last a few minutes.[medicinenet.com]

    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
  • Transient Ischemic Attack

    These symptoms include: Confusion or memory problems Difficulty understanding speech or sudden speech impairment, such as slurred speech Facial paralysis Sudden leg or arm[loyolamedicine.org] Often there is a facial droop.[medicinenet.com] Arms: Arm weakness or numbness might make it hard for the individual to either raise both arms or to keep them raised. Speech: Speech may be slurred and garbled.[medicalnewstoday.com]

    Missing: Mutation in the Tight Junction Protein 2 Gene
  • Traumatic Brain Injury

    […] or tingling Droopy eyelid or facial weakness Loss of bowel control or bladder control If a TBI is suspected, call 911 immediately or take the person to an emergency room.[aans.org] Cognitive difficulties Inappropriate emotional responses Speech difficulties (slurred speech, inability to understand and/or articulate words) Difficulty swallowing Body numbness[aans.org]

    Missing: Mutation in the Tight Junction Protein 2 Gene
  • Brain Neoplasm

    Tumors in or near other cranial nerves might lead to hearing loss (in one or both ears), balance problems, weakness of some facial muscles, facial numbness or pain, or trouble[cancer.org] Progressive dizziness and unilateral facial numbness are also common. Neurofibromatosis type 2, a rare autosomal dominant disorder, is a strong risk factor.[bestpractice.bmj.com] These tumors can cause visual problems, loss of sensation in the face, or facial numbness.[brighamandwomens.org]

    Missing: Mutation in the Tight Junction Protein 2 Gene
  • Cerebral Hemorrhage

    […] paralysis Numbness or tingling Vision changes Any change in vision Decreased vision, loss of all or part of vision Double vision Eyelid drooping Pupils different size Uncontrollable[snc.md] Facial paralysis can be seen, too. Sensorial disorder: are seen as single or double-sided. Numbness or burning-like feeling occurs in the Face, arms, legs and body.[groupflorence.com] Difficulty moving any body part Hand tremor Loss of fine motor skills Weakness of any body part Nausea, vomiting Seizure Sensation changes Abnormal sensations Decreased sensation Facial[snc.md]

    Missing: Mutation in the Tight Junction Protein 2 Gene
  • Ischemic Stroke

    An otherwise healthy 30-year-old black man presented with headache for about 3 hours, left-sided facial and upper extremity numbness, slurred speech, miosis, lacrimation,[ncbi.nlm.nih.gov]

    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]

    Missing: Focal Polymorphic Delta Slowing
  • Hyperventilation

    Hyperventilation exercise during electroencephalography precipitated a recurrence of right hemiplegia and aphasia in a patient with Hb SS disease. Although recovery of function started within hours of the event, full recovery has not occurred six months after. Hyperventilation provocative test during[…][ncbi.nlm.nih.gov]

    Missing: Focal Polymorphic Delta Slowing Mutation in the Tight Junction Protein 2 Gene
  • 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: Focal Polymorphic Delta Slowing Mutation in the Tight Junction Protein 2 Gene