Create issue ticket

214 Possible Causes for Ileocecal, recess

  • Adrenal Insufficiency

    Here, we have performed whole exome sequencing to identify recessive causes of SRNS.[] Called also myocardial ischemia . ileocecal insufficiency inability of the ileocecal valve to prevent backflow of contents from the cecum into the ileum. placental insufficiency[] Abstract Allgrove syndrome or triple-Asyndrome is a rare familial multisystem autosomal recessive disorder.[]

  • Tuberculosis

    […] to mycobacterial infection; this predisposition, which had resulted in death in three children and chronic mycobacterial infection in a fourth, was felt to be autosomal recessive[] There is a predilection for ileocecal involvement because of the abundant lymphoid tissue and slower rate of passage of lumenal contents.[] Hoeffel C, Crema MD, Belkacem A, et al.: Multi-detector row CT: spectrum of diseases involving the ileocecal area. Radiographics 2006, 26:1373–1390.[]

  • Ileocecal Tuberculosis

    The caecal recess may be more or less retracted or amputated such that the terminal ileum continuous without apparent transition into the ascending colon.[] Abstract The diagnosis of ileocecal tuberculosis requires roentgenologic confirmation.[] Abstract Three cases of ileocecal tuberculosis are presented with a review of pathogenesis, diagnosis and therapy.[]

  • Kohlschütter-Tönz Syndrome

    […] diseases Search Search for a rare disease Amelocerebrohypohidrotic syndrome Disease definition Kohlschütter-Tönz syndrome (KTS) is a genetically heterogeneous autosomal recessive[] Small intestine (intestinum tenue)extends from pylorus to ileocecal junctionparts: duodenum jejunum ileummain function:absorbtion of nutrientsplicae circulares(circular folds[] Occasionally recessive mutations are identified: a recent publication described a distinct neonatal epileptic encephalopathy (MIM 615905) caused by autosomal recessive mutations[]

  • Intussusception

    Abstract Glanzmann's thrombasthenia (GT) is a rare autosomal recessive disorder in which the platelets have anomalies of fibrinogen receptors causing bleeding tendencies.[] The authors describe an unusual case of mucosa-associated lymphoid tissue (MALT) lymphoma as the underlying cause of ileocecal intussusception in an elderly woman.[] Clinical and radiologic findings suggested ileocecal intussusception initially.[]

  • Hereditary Multiple Intestinal Atresia

    The inheritance of the severe combined immunodeficiency syndrome can be autosomal recessive or X‐linked. We report on 3 sibs with multiple‐level intestinal atresias.[] Also, colic atresia and ileocecal atresia were treated with an " en bloc " resection, including cecal appendix, using a gastro-intestinal anastomosis stapler and creating[] Attempts to reflux contrast into the terminal ileum beyond the ileocecal valve were unsuccessful.[]

  • Primary Ciliary Dyskinesia

    Primary ciliary dyskinesia (PCD) is a genetic disease inherited in an autosomal recessive manner. The prevalence of PCD is estimated to be 1 in 20,000 live births.[] The arm is thus distinguished in medical usage from the forearm … Medical dictionary ICS — ileocecal sphincter; image criteria score; immotile cilia syndrome; immunocytochemical[] Abstract Primary ciliary dyskinesia (PCD) is an autosomal recessive heterogeneous group of conditions with variable clinical findings like recurrent respiratory tract infections[]

  • Megacystis - Microcolon - Intestinal Hypoperistalsis Syndrome

    These cases further support the view that this syndrome is inherited in an autosomal recessive fashion.[] 751.5 intestine (large) (small) 751.5 Anomaly, anomalous (congenital) (unspecified type) 759.9 anus, anal (canal) 751.5 appendix 751.5 cecum 751.5 colon 751.5 duodenum 751.5 ileocecal[] These cases, together with three other published reports of affected sibs, confirm the autosomal recessive inheritance of the syndrome.[]

  • Cecal Volvulus

    Abstract Alström syndrome (ALMS1, MIM 203800) is a rare, autosomal recessively inherited monogenic condition caused by mutations in the ALMS1 gene located on the short arm[] Whirl, ileocecal twist, transition points, X-marks-the-spot, and split wall have high specificity for cecal volvulus.[] We therefore conducted an ileocecal resection.[]

  • Autosomal Dominant Hyper-IgE Syndrome

    Autosomal recessive hyper-IgE syndrome with atypical mycobacteriosis definition of autosomal recessive hyper-IgE syndrome with atypical mycobacteriosis by Medical dictionary[] PubMed Google Scholar Alberti-Flor JJ, Granda A: Ileocecal histoplasmosis mimicking Crohn's disease in a patient with Job's syndrome.[] HIES, Job's syndrome (disorder), Syndrome, Hyper-IgE, Syndrome, Job's, Hyper Immunoglobulin E Syndrome, Autosomal Recessive, Autosomal Recessive HIESs, HIESs, Autosomal Recessive[]

Further symptoms