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214 Possible Causes for Ileocecal, recess

  • Adrenal Insufficiency

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

  • 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[emedicine.com] There is a predilection for ileocecal involvement because of the abundant lymphoid tissue and slower rate of passage of lumenal contents.[library.med.utah.edu] Hoeffel C, Crema MD, Belkacem A, et al.: Multi-detector row CT: spectrum of diseases involving the ileocecal area. Radiographics 2006, 26:1373–1390.[dx.doi.org]

  • 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.[jpma.org.pk] Abstract The diagnosis of ileocecal tuberculosis requires roentgenologic confirmation.[pubs.rsna.org] Abstract Three cases of ileocecal tuberculosis are presented with a review of pathogenesis, diagnosis and therapy.[ncbi.nlm.nih.gov]

  • Kohlschütter-Tönz Syndrome

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

  • Intussusception

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

  • 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.[doi.org] Also, colic atresia and ileocecal atresia were treated with an " en bloc " resection, including cecal appendix, using a gastro-intestinal anastomosis stapler and creating[synapse.koreamed.org] Attempts to reflux contrast into the terminal ileum beyond the ileocecal valve were unsuccessful.[nature.com]

  • 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.[ncbi.nlm.nih.gov] The arm is thus distinguished in medical usage from the forearm … Medical dictionary ICS — ileocecal sphincter; image criteria score; immotile cilia syndrome; immunocytochemical[translate.academic.ru] Abstract Primary ciliary dyskinesia (PCD) is an autosomal recessive heterogeneous group of conditions with variable clinical findings like recurrent respiratory tract infections[ncbi.nlm.nih.gov]

  • Megacystis - Microcolon - Intestinal Hypoperistalsis Syndrome

    These cases further support the view that this syndrome is inherited in an autosomal recessive fashion.[ncbi.nlm.nih.gov] 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[icd9data.com] These cases, together with three other published reports of affected sibs, confirm the autosomal recessive inheritance of the syndrome.[ncbi.nlm.nih.gov]

  • 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[ncbi.nlm.nih.gov] Whirl, ileocecal twist, transition points, X-marks-the-spot, and split wall have high specificity for cecal volvulus.[ncbi.nlm.nih.gov] We therefore conducted an ileocecal resection.[ncbi.nlm.nih.gov]

  • 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[medical-dictionary.thefreedictionary.com] PubMed Google Scholar Alberti-Flor JJ, Granda A: Ileocecal histoplasmosis mimicking Crohn's disease in a patient with Job's syndrome.[ojrd.biomedcentral.com] HIES, Job's syndrome (disorder), Syndrome, Hyper-IgE, Syndrome, Job's, Hyper Immunoglobulin E Syndrome, Autosomal Recessive, Autosomal Recessive HIESs, HIESs, Autosomal Recessive[ebi.ac.uk]

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