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138 Possible Causes for Autosomal Dominant, Occult Blood Positive, Pediatric Disorder

  • Familial Adenomatous Polyposis

    If screened after a positive fecal occult blood test result, the prevalence increases to 0.34% to 0.66%. [31] International Worldwide studies of Gardner syndrome kindreds[emedicine.medscape.com] English familial adenomatous polyposis autosomal dominant disease that is has material basis in mutations in the APC gene and involves formation of numerous polyps in the[wikidata.org] In conclusion, FAP is a systemic disorder with significant implications for affected patients and family members.[journals.lww.com]

  • Gardner Syndrome

    Affiliation: Discipline of Pediatric Otorhinolaryngology, Department of Otorhinolaryngology and Human Communication Disorders, EPM – UNIFESP[scielo.br] Physical examination reveals multiple epidermal inclusion cysts and a fecal occult blood test is positive. Colonoscopy reveals innumerable colonic polyps.[prep4usmle.com] Gardner syndrome, a variant of familial adenomatous polyposis, is an autosomal dominant genetic disease characterized by the combined presence of multiple intestinal polyps[ncbi.nlm.nih.gov]

  • Juvenile Polyp

    A fecal occult blood test was positive. Results of stool viral and bacterial studies were negative. She was started on iron supplementation.[consultant360.com] Wireless capsule endoscopy for oscure small-bowel disorders: Final results of the first pediatric controlled trial . Clin Gastroenterol Hepatol 2005; 3 :264–270. 21.[nature.com] An autosomal dominant condition usually associated with mutations in 2 genes – BMPRIA (bone morphogenic protein receptor, type 1A) and SMAD4 (mothers against decapentaplegic[ajol.info]

  • Hereditary Hemorrhagic Telangiectasia

    The monoclonal antibody bevacizumab, seems to be a good option in this disorder.[ncbi.nlm.nih.gov] Fecal occult blood testing can be falsely positive due to swallowed blood from nosebleeds, and hence, is less useful as a screening.[dovepress.com] BACKGROUND AND OBJECTIVE: Pulmonary arterial hypertension (PAH) is a rare disease that could be inherited with an autosomal dominant pattern.[ncbi.nlm.nih.gov]

  • Peutz-Jeghers Syndrome

    […] risks separately, with the latter disorders discussed in the article by Tabori and colleagues in this CCR Pediatric Oncology Series ( 1 ).[dx.doi.org] From Wikidata Jump to navigation Jump to search autosomal dominant genetic disorder characterized by the development of benign hamartomatous polyps in the gastrointestinal[wikidata.org] Peutz-Jeghers syndrome (PJS) is a rare autosomal dominant disorder characterized by mucocutaneous hyperpigmentation, gastrointestinal (GI) hamartmatous polyps, and an increased[ncbi.nlm.nih.gov]

  • Von Willebrand Disease

    John Akabutu Comprehensice Centre for Bleeding DisordersPediatric Division Stollery Children’s Hospital Clinic Director Dr.[hemophilia.ca] Type 2B von Willebrand disease is also an autosomal dominant trait.[emedicine.medscape.com] Warad, Pediatric Coagulation Disorders, Pediatrics in Review, 37, 7, (279), (2016).[doi.org]

  • Ehlers-Danlos Syndrome

    The paucity of patients described so far makes this disorder poorly defined at clinical level.[ncbi.nlm.nih.gov] DOMINANT EHLERS-DANLOS SYNDROME, TYPE V EHLERS-DANLOS SYNDROME, TYPE VI EHLERS-DANLOS SYNDROME, TYPE VII, AUTOSOMAL DOMINANT EHLERS-DANLOS SYNDROME, TYPE VII, AUTOSOMAL RECESSIVE[web.archive.org] Marco Castori and Alan Hakim, Contemporary approach to joint hypermobility and related disorders, Current Opinion in Pediatrics, 10.1097/MOP.0000000000000541, 29, 6, (640-[doi.org]

  • Blue Rubber Bleb Nevus Syndrome

    Phone: 617-636-5025 Fax #: 617-636-8122 Pediatric surgery, pediatric trauma, congenital disorders requiring surgery in newborns, GI inflammatory diseases in children, pediatric[floatinghospital.org] Fecal occult blood test was positive. Bone marrow aspiration revealed myeloid hyperactivity and normocellular marrow with minimal erythroids.[doi.org] "Blue rubber bleb nevus syndrome" is an autosomal dominant trait characterized by multiple cutaneous and extracutaneous angiomas of dark blue color and rubbery consistency[ncbi.nlm.nih.gov]

  • Meckel Syndrome

    […] in children Health Articles See all » Treatments for Pediatric Spinal Deformities Infrared Therapy: Health Benefits and Risks Everything You Need to Know About Giving Up[news-medical.net] Abstract Autosomal dominant mutations in the SFTPC gene are associated with idiopathic pulmonary fibrosis, a progressive lethal interstitial lung disease.[ncbi.nlm.nih.gov] Avni, Prenatal sonographic patterns in autosomal dominant polycystic kidney disease: a multicenter study, Ultrasound in Obstetrics & Gynecology, 24, 1, (55-61), (2004).[doi.org]

  • Sickle Cell Disease

    Elder and Jeremie Heath Estepp, Hematologic Disorders of the Eye, The Eye in Pediatric Systemic Disease, 10.1007/978-3-319-18389-3_11, (295-325), (2017).[doi.org] See illustration at cell. sickle cell anemia an autosomal dominant, chronic form of hemolytic anemia in which large numbers of sickle cells circulate in the blood; it is most[medical-dictionary.thefreedictionary.com] Center, Children's Healthcare of Atlanta, Emory University, Atlanta, Georgia. 4 Department of Pediatrics, Yale University, New Haven, Connecticut. 5 Department of Laboratory[ncbi.nlm.nih.gov]

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