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2,051 Possible Causes for Facial Numbness, Hypokalemic Periodic Paralysis, 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] periodic paralysis 低カリウム性周期性四肢麻痺 hypokinesia 運動低下/運動不足 hypomagnesemia 低マグネシウム血症/低マグネシウム血 hypomagnesemic tetany 低マグネシウム血性テタニー hyponatremia 低ナトリウム血症 hyponatremic dehydration[jpeds.or.jp] Herein, we report 2 sisters with FHHNC. Both sisters presented at an early stage with hypomagnesemia and hypocalcemia.[ncbi.nlm.nih.gov]

  • Acute Hyperventilation

    Severe prognosis in a large family with hypokalemic periodic paralysis. Muscle Nerve 2003 ; 27 : 165 –9 8 Geffner I, Murgatroyd J. Tetany.[academic.oup.com] Conditions such as periodic paralysis occur because of changes in serum potassium and lead to hypotonic or flaccid paralysis. 7 No change in serum potassium was found in this[academic.oup.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
  • Anxiety Disorder

    Anxiety can be an appropriate response to stressful situations but is considered a pathologic disorder when it is disabling and difficult to control. Generalized anxiety disorder (GAD) is the most common anxiety disorder seen in primary care, affecting approximately 3% of adults in the United States (1, 2). This[…][doi.org]

    Missing: Mutation in the Tight Junction Protein 2 Gene
  • Conversion Disorder

    A' who was experiencing myriad symptoms which included tremors, facial numbness, and severe headaches.[study.com] Doctors may test for health problems such as: Stroke, epilepsy, hypokalemic periodic paralysis, or multiple sclerosis.[psychcentral.com] […] from hypokalemic periodic paralysis. [14] Misdiagnosis does sometimes occur.[en.wikipedia.org]

    Missing: Mutation in the Tight Junction Protein 2 Gene
  • Primary Progressive Multiple Sclerosis

    Facial numbness and weakness are also common.[medical-dictionary.thefreedictionary.com] 遺伝性周期性四肢麻痺 Periodic paralysis 周期性四肢麻痺 1 不要 HPS1062 HPS1063 HPS1064 HPS1065 117. 脊髄空洞症 Syringomyelia 脊髄空洞症 1 不要 有 HPS2285 HPS2286 HPS2287 HPS2288 HPS2289 119.[cell.brc.riken.jp]

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

    numbness, and new facial numbness.[ro-journal.biomedcentral.com] paralysis ( Hypokalemic, Hyperkalemic ) - Lambert-Eaton myasthenic syndrome Cerebral palsy والمتلازمات paralytic الأخرى Cerebral palsy - Paralysis - Spastic diplegia - Hemiplegia[marefa.org] Microvascular decompression has some risks, including decreased hearing, facial weakness, facial numbness, a stroke or other complications.[mayoclinic.org]

    Missing: Mutation in the Tight Junction Protein 2 Gene
  • Guillain-Barré Syndrome

    Diagnosis is made by the clinical features of the disease: muscle weakness of extremities, facial palsy, pain, and numbness of fingers and toes.[symptoma.com] Periodic Paralysis , see Hypokalemic periodic paralysis Familial idiopathic basal ganglia calcification familial idiopathic cardiomyopathy , see Familial dilated cardiomyopathy[herenciageneticayenfermedad.blogspot.com] Demonstrable altered sensation or numbness. Reduced or absent reflexes. Fasciculation may occasionally be noted. Facial weakness - may be asymmetrical.[patient.info]

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

    numbness Reduced rate of respiration is one of the initial symptoms of this condition.[hxbenefit.com] […] insipidus ( E23.2 ) electrolyte imbalance associated with hyperemesis gravidarum ( O21.1 ) electrolyte imbalance following ectopic or molar pregnancy ( O08.5 ) familial periodic[icd10data.com] […] semiconsciousness or even coma Lightheadedness Irritability Prolonged spasms in the muscles ( Tetany ) Twitching of the muscles Vomiting Nausea Tingling sensations in the face Facial[hxbenefit.com]

    Missing: Mutation in the Tight Junction Protein 2 Gene
  • Myasthenia Gravis

    Later that month, the patient was admitted to the hospital with constipation, worsening nausea and vomiting, right arm and hand numbness and paresthesia, and a worsening occipital[sciencerepository.org] Neurological examination was notable for mild diplopia on sustained up-gaze without ptosis or other facial weakness, as well as decreased proprioception and slowed rapid alternating[sciencerepository.org]

    Missing: Mutation in the Tight Junction Protein 2 Gene

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