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105 Possible Causes for Ileocaecal, recess

  • Short Bowel Syndrome

    MATERIALS AND METHODS: A 3-year-old girl suffered subtotal loss of her small bowel and ileocaecal junction as a result of midgut volvulus.[] Pathogenic variants in CLMP were recently identified to cause an autosomal recessive form of the disease.[] Gastroschisis had the lowest rate of preserved ileocaecal valve (10%), while intestinal atresia had the highest (66%).[]

  • Malignant Neoplasm

    The small intestine is defined as the proximal portion of the intestine comprising the duodenum, jejunum and ileum, excluding the pyloric opening of the stomach and the ileocaecal[] […] recurrence rates in endoscopically resected inverted papilloma (IP) and recommended external surgery for inverted papilloma (IP) that extends into the frontal sinus, supraorbital recess[] […] the beginning of this chapter] C16.9 Stomach, unspecified Gastric cancer NOS C17 Malignant neoplasm of small intestine C17.0 Duodenum C17.1 Jejunum C17.2 Ileum Excludes: ileocaecal[]

  • Intussusception

    This condition most often occurs in the ileocaecal region.[] Abstract Glanzmann's thrombasthenia (GT) is a rare autosomal recessive disorder in which the platelets have anomalies of fibrinogen receptors causing bleeding tendencies.[] In most children the intussusception is ileocaecal, although ileo-ileocolic and ileo-ileal or colocolic cases can occur.[]

  • Crohn's Disease

    After complementary study, a mild ileocaecal involvement of CD was demonstrated. The patient became asymptomatic with proton pump inhibitor and a course of prednisolone.[] Although a high redilatation rate is one of the clinical problems of this procedure, EBD is an effective therapy for avoiding intestinal recession in CD -stricture. 2018 S[]

  • Henoch-Schönlein Purpura

    Because of protracted gastro-intestinal bleeding after initiating therapy with methylprednisolone and ileocaecal resection, azathioprine was started.[] We also showed that rs1927914 variant decreased the risk of HSP in recessive inheritance model (OR 0.55; p 0.035, G/G vs A/A A/G).[]

  • Liver Cirrhosis

    We report the case of a 56-year-old woman with ileocaecal Crohn's disease treated with azathioprine.[] Abstract Alström syndrome is a rare autosomal recessive genetic disorder characterized by cone-rod dystrophy, hearing loss, childhood truncal obesity, insulin resistance and[] RATIONALE: Progressive familial intrahepatic cholestasis (PFIC) type 3, characterized by high gamma glutamyl transferase (GGT), is an autosomal recessive genetic disease.[]

  • Abdominal Mass

    Right iliac fossa Actinomycosis Amoebic abscess Appendix mass or abscess Caecal/colon cancer or distension Crohn's disease (multiple tender, sausage-shaped masses) Hernia Ileocaecal[] Bilateral renal masses detected on examination or imaging are concerning for autosomal recessive polycystic kidney disease (ARPKD).[] […] obstruction Note: sever hydro can be detected in utero and treated with a uretero-amniotic shunt Multicystic Kidney Unilateral: multicystic dysplastic kidney Bilateral Autosomal recessive[]

  • Gastrointestinal Stromal Tumor

    Exploratory laparotomy revealed a mass originating from ileocaecal region.[] When familial GIST is associated with mutations in other genes, it can have an autosomal recessive pattern of inheritance , which means alterations in both copies of the gene[] Two of the cases were located in the stomach, one in the duodenum involving the periampullary area, one each ileocaecal region, transverse colon and rectum.[]

  • Small Intestinal Bacterial Overgrowth

    […] migrating motor complex (MMC) is responsible for the flow of bacteria into the large bowel during periods of fasting, Other protective mechanisms include the functional ileocaecal[] Objective: Familial Mediterranean fever (FMF) is an autosomal recessive disease due to a MEFV gene mutation.[]

  • Common Variable Immunodeficiency

    We present the case of a patient with common variable immunodeficiency suffering a chronic diarrhea episode and who was diagnosed with ileocaecal Crohn s-like disease after[] METHODS: A patient given a diagnosis of CVID, who was born to a consanguineous family and thus would be expected to show an autosomal recessive inheritance, was subjected[] […] had a specific signature in clinical presentation and immunologic profile, and a high consanguinity in this group of patients suggests a Mendelian trait with an autosomal recessive[]

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