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689 Possible Causes for Abdominal Cramps, Autosomal Dominant, Pediatric Disorder

  • Gardner Syndrome

    Affiliation: Discipline of Pediatric Otorhinolaryngology, Department of Otorhinolaryngology and Human Communication Disorders, EPM – UNIFESP[scielo.br] Passage of blood or mucosa, diarrhea, and cramp-like abdominal pain are the common presenting symptoms. [4] The present case also had a complaint of abdominal cramps.[contempclindent.org] 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]

  • Acute Hepatic Porphyria

    Tortorelli S, Kloke K, Raymond K: Chapter 15: Disorders of porphyrin metabolism. In Biochemical and Molecular Basis of Pediatric Disease. Fourth edition.[mayomedicallaboratories.com] Most important symptoms are related to the gastrointestinal tract and include intense and nonspecific abdominal pain that may be cramping, constipation, nausea, vomiting,[symptoma.com] Masters suggested Ryan's abdominal bleeding might be caused by acute intermittent porphyria, but there were no abdominal cramps to go along with it.[house.wikia.com]

  • 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] cramping, intussusception, chronic bleeding, anemia due to chronic blood loss Peutz-Jeg·hers syn·drome (PJS) ( pŭts jā'gĕrz sindrōm ) Generalized hamartomatous multiple polyposis[medical-dictionary.thefreedictionary.com] 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]

  • Erythropoietic Coproporphyria

    Tortorelli S, Kloke K, Raymond K: Chapter 15: Disorders of porphyrin metabolism. In Biochemical and Molecular Basis of Pediatric Disease. Fourth edition.[mayomedicallaboratories.com] Masters suggested Ryan's abdominal bleeding might be caused by acute intermittent porphyria, but there were no abdominal cramps to go along with it.[house.wikia.com] dominant ) Hereditary coproporphyria ( autosomal dominant ) Doss porphyria ( autosomal recessive ) Chronic hepatic porphyrias Porphyria cutanea tarda ; ( autosomal dominant[amboss.com]

  • Lactose Intolerance

    Lactose Intolerance, in Pediatric Nutrition in Chronic Diseases and Developmental Disorders, 2nd ed. Walberg Ekvall S and Ekvall VK, eds.[labtestsonline.org] Challenge at week 4 for diarrhea (p   0.033), abdominal cramping (p   0.012), vomiting (p   0.0002), and overall symptom score (p   0.037).[ncbi.nlm.nih.gov] The variations that promote continued lactase production are considered autosomal dominant, which means one copy of the altered regulatory element in each cell is sufficient[ghr.nlm.nih.gov]

  • Familial Adenomatous Polyposis

    Older paternal age and fresh gene mutation: data on additional disorders. J Pediatr. 1975 Jan. 86(1):84-8. [Medline]. Bisgaard ML, Fenger K, Bülow S, Niebuhr E, Mohr J.[emedicine.medscape.com] cramps – Unexplained, significant weight loss ( 10%) – Blood in your stool Maintain a high-fiber diet that is low in fat and calories; consult your physician for proper diet[ameripath.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]

  • Fabry Disease

    , and the Society for Pediatric Research.[books.google.de] Autonomic small fiber damage in Fabry disease is likely to be related to the patients' gastrointestinal dysmotility (e.g., abdominal cramps, bloating, diarrhea, nausea), hypohidrosis[ncbi.nlm.nih.gov] The cysts are perhaps the most specific sign, typically small and of uniform size, located just beneath the capsule, aiding in differentiating these from autosomal dominant[radiopaedia.org]

  • Malabsorption Syndrome

    Copyright 1985 by the American Academy of Pediatrics Log in using your username and password Log in through your institution You may be able to gain access using your login[pediatrics.aappublications.org] Signs and symptoms include bloody diarrhea, abdominal cramping and pain on the left side, and unintended weight loss. 113.  Pancolitis.[slideshare.net] Case 51 yo F w/ ESRD of autosomal dominant polycystic kidney disease 76 yo M w/ ESRD of an unknown etiology 37 yo M w/ ESRD of an unknown etiology 66 yo M w/ orthotopic liver[omicsonline.org]

  • Juvenile Polyp

    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] When the polyps are large or numerous, things you might notice include: Bleeding from the rectum Blood in your stool Diarrhea Constipation Cramping/abdominal pain Anemia -[my.clevelandclinic.org] 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]

  • 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] Case Report A 36-year-old man presented with abdominal cramps, diarrhoea and several episodes of profuse rectal bleeding of 1 week duration.[ispub.com] "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]

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