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149 Possible Causes for Mutation in the WWOX Gene, Pollakisuria

  • Epithelial Ovarian Cancer

    TP53 and PTEN are among the best known tumor suppressor genes involved in EOC pathogenesis, but mutations have also been found in genes OPCML and WWOX, among others.[symptoma.com] Characteristic yet unspecific symptoms of EOC comprise abdominal or pelvic pain, early satiety, bloating, urinary urgency and pollakisuria.[symptoma.com]

  • Urinary Tract Infection

    The following factors have been established from clinical studies ( 7, 8 ): • Dysuria, pollakisuria, nycturia ( ) • Present or increased incontinence ( ) • Macrohematuria[dx.doi.org] The following factors have been established from clinical studies ( 7, 8 ): Dysuria, pollakisuria, nycturia ( ) Present or increased incontinence ( ) Macrohematuria ( ) Suprapubic[ncbi.nlm.nih.gov]

    Missing: Mutation in the WWOX Gene
  • Acute Cystitis

    The following factors have been established from clinical studies ( 7, 8 ): • Dysuria, pollakisuria, nycturia ( ) • Present or increased incontinence ( ) • Macrohematuria[dx.doi.org] The following factors have been established from clinical studies ( 7, 8 ): Dysuria, pollakisuria, nycturia ( ) Present or increased incontinence ( ) Macrohematuria ( ) Suprapubic[ncbi.nlm.nih.gov]

    Missing: Mutation in the WWOX Gene
  • Cystitis

    Cystitis is a condition, characterized by inflammation of the bladder, which majorly occurs due to bacterial infection. It is a common form of lower urinary tract infection. The condition of cystitis presents itself with the following signs and symptoms: Dysuria Increase in urge to urinate Development of hematuria[…][symptoma.com]

    Missing: Mutation in the WWOX Gene
  • Constipation

    Importance of the field: Chronic constipation has a high prevalence, and current medical and pharmacological therapies do not restore normal bowel function in all patients. Areas covered in the review: A PubMed search (1965 – 2009) using the following terms alone or in combination: prucalopride, 5-HT 4, R093877,[…][oadoi.org]

    Missing: Mutation in the WWOX Gene
  • Ovarian Cyst

    2015 ICD-9-CM Diagnosis Code 620.2 Other and unspecified ovarian cyst 2015 Billable Thru Sept 30/2015 Non-Billable On/After Oct 1/2015 Female Only Dx ICD-9-CM 620.2 is a billable medical code that can be used to indicate a diagnosis on a reimbursement claim, however, 620.2 should only be used for claims with a date of[…][icd9data.com]

    Missing: Mutation in the WWOX Gene
  • Pregnancy

    Pregnancy in patients with end-stage renal disease is rare, with a paucity of management guidelines in the literature. Various hemodialysis (HD) and peritoneal dialysis (PD) protocols have been used to successfully manage pregnancy in this population; however, there is a growing body of evidence that the best[…][ncbi.nlm.nih.gov]

    Missing: Mutation in the WWOX Gene
  • Benign Prostatic Hyperplasia

    To examine utilization and costs of care for benign prostatic hyperplasia (BPH)-related services in a large cohort of commercially insured persons. Pharmacy and medical claims data were obtained from 61 US healthcare plans. Men aged or 45 years who were newly diagnosed with BPH between January 2000 and March[…][ncbi.nlm.nih.gov]

    Missing: Mutation in the WWOX Gene
  • Urethritis

    The purpose of the present study was to determine pathogens and behaviors associated with nongonococcal urethritis (NGU) and the usefulness of the urethral smear in predicting the presence of pathogens. We conducted a case-control study of men with and without symptoms of NGU. Sexual practices were[…][ncbi.nlm.nih.gov]

    Missing: Mutation in the WWOX Gene
  • Salpingitis

    A case of xanthogranulomatous salpingitis and oophoritis in a 47-year-old woman is presented. Xanthogranulomatous inflammation is an uncommon form of chronic inflammation that is destructive to affected organs; it is characterized by the presence of lipid-filled macrophages with admixed lymphocytes, plasma cells,[…][ncbi.nlm.nih.gov]

    Missing: Mutation in the WWOX Gene

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