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97 Possible Causes for Disorganized Slow Background Activity, Mutation in the WWOX Gene

  • Early Infantile Epileptic Encephalopathy Type 28

    Homozygous and compound heterozygous mutations in the WWOX gene (16q23) have been found in several families.[disorders.eyes.arizona.edu] Homozygous mutations involving the WWOX gene were found on whole exome sequencing in both cases (deletion affecting exons 3 to 4 in case one, and splice-site mutation c.606[omicsonline.org] He was diagnosed last november with a rare mutation in the WWOX gene causing him to have EIEE28, early infantile epileptic encephalopathy.[medhelp.org]

  • Hypoglycemia

    Intern Med. 2016;55(8):949-53. doi: 10.2169/internalmedicine.55.5737. Epub 2016 Apr 15. Author information 1 Department of Endocrinology and Metabolism, Dokkyo Medical University, Japan. Abstract We encountered a 62-year-old woman who experienced frequent episodes of hypoglycemia. She was diagnosed with postprandial[…][ncbi.nlm.nih.gov]

    Missing: Mutation in the WWOX Gene
  • Hyponatremia

    OBJECTIVES: To assess symptoms and characteristics of hyponatremia, the most common electrolyte disturbance in hospitalized individuals and a condition that is associated with substantial morbidity and mortality. DESIGN: Prospective observational multicenter study. SETTING: Two Swiss academic centers. PARTICIPANTS:[…][ncbi.nlm.nih.gov]

    Missing: Mutation in the WWOX Gene
  • Alzheimer Disease

    Although the neuropathologic changes and diagnostic criteria for the neurodegenerative disorder Alzheimer's disease (AD) are well-established, the clinical symptoms vary largely. Symptomatically, frontal variant of AD (fv-AD) presents very similarly to behavioral variant frontotemporal dementia (bvFTD), which creates[…][ncbi.nlm.nih.gov]

    Missing: Mutation in the WWOX Gene
  • Traumatic Brain Injury

    Pediatric head injuries are common and may present with varying degrees of altered mental status in children. The approach to evaluation, diagnosis, treatment, and prevention of further injury is important in achieving good health outcomes after a head injury. In this article, we review the pathophysiology,[…][ncbi.nlm.nih.gov]

    Missing: Mutation in the WWOX Gene
  • Stroke

    BACKGROUND: Impaired gait function after stroke contributes strongly to overall patient disability. Recently, sleep disturbance was reported to negatively affect functional recovery after stroke. OBJECTIVE: The aim of this study was to identify the impact of sleep disturbance on balance and gait function in stroke[…][ncbi.nlm.nih.gov]

    Missing: Mutation in the WWOX Gene
  • Dementia

    † Deceased. From University of Minnesota, Minneapolis, Minnesota; Brown University, Providence, Rhode Island; and Minneapolis VA Health Care System and HealthPartners, Minneapolis, Minnesota. Disclaimer: Findings and conclusions are those of the authors, who are responsible for the article's contents; findings and[…][doi.org]

    Missing: Mutation in the WWOX Gene
  • Cushing Syndrome

    Adrenal oncocytoma is very rare pathological variant of adrenal neoplasm. These are usually large and non-functional; however, rarely functional adrenal oncocytomas are also presented as Cushing's syndrome and pheochromocytoma. We report a case of adrenal oncocytoma in 38 year old female presented with symptoms[…][ncbi.nlm.nih.gov]

    Missing: Mutation in the WWOX Gene
  • Meningoencephalitis

    Ital J Pediatr. 2015 Jan 20;41:3. doi: 10.1186/s13052-014-0107-1. Author information 1 Department of Pediatrics, The Second Affiliated Hospital and Yuying Children's Hospital of Wenzhou Medical University, 109 West Xueyuan Road, Wenzhou, China. zhouyonghai311@126.com. Abstract The most usual presentation of Plesiomonas[…][ncbi.nlm.nih.gov]

    Missing: Mutation in the WWOX Gene
  • Hydrocephalus

    A 39-year old man underwent surgery for recurrence of a cervical schwannoma. At 6 months postoperatively, severe headache appeared and head CT showed marked ventricular dilation that was diagnosed as delayed hydrocephalus. Dural repair surgery using a fascia patch of the tensor fasciae latae muscle was[…][ncbi.nlm.nih.gov]

    Missing: Mutation in the WWOX Gene

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