prikaz prve stranice dokumenta Down syndrome and Crohn’s disease: An extremely rare association
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Scientific paper - Case study
Down syndrome and Crohn’s disease: An extremely rare association
Pediatrics International, 43 (2001), 5; 519-521. https://doi.org/10.1046/j.1442-200X.2001.01431.x
Peršić, Mladen; Dessardo, Sandro; Šubat-Dežulović, Mirna; Ahel, Vladimir; Rožmanić, Vojko

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Peršić, M., Dessardo, S., Šubat Dežulović, M., Ahel, V. & Rožmanić, V. (2001). Down syndrome and Crohn’s disease: An extremely rare association. Pediatrics International, 43. (5), 519-521. doi: 10.1046/j.1442-200X.2001.01431.x

Peršić, Mladen, et al. "Down syndrome and Crohn’s disease: An extremely rare association." Pediatrics International, vol. 43, no. 5, 2001, pp. 519-521. https://doi.org/10.1046/j.1442-200X.2001.01431.x

Peršić, Mladen, Sandro Dessardo, Mirna Šubat Dežulović, Vladimir Ahel and Vojko Rožmanić. "Down syndrome and Crohn’s disease: An extremely rare association." Pediatrics International 43, no. 5 (2001): 519-521. https://doi.org/10.1046/j.1442-200X.2001.01431.x

Peršić, M., et al. (2001) 'Down syndrome and Crohn’s disease: An extremely rare association', Pediatrics International, 43(5), pp. 519-521. doi: 10.1046/j.1442-200X.2001.01431.x

Peršić M, Dessardo S, Šubat Dežulović M, Ahel V, Rožmanić V. Down syndrome and Crohn’s disease: An extremely rare association. Pediatrics International [Internet]. 2001 October 05 [cited 2024 May 03];43(5):519-521. doi: 10.1046/j.1442-200X.2001.01431.x

M. Peršić, S. Dessardo, M. Šubat Dežulović, V. Ahel and V. Rožmanić, "Down syndrome and Crohn’s disease: An extremely rare association", Pediatrics International, vol. 43, no. 5, pp. 519-521, October 2001. [Online]. Available at: https://urn.nsk.hr/urn:nbn:hr:184:996970. [Accessed: 03 May 2024]

Metadata
Title (english)Down syndrome and Crohn’s disease: An extremely rare association
AuthorMladen Peršić
AuthorSandro Dessardo
AuthorMirna Šubat-Dežulović
AuthorVladimir Ahel
AuthorVojko Rožmanić
Author's institutionUniversity of Rijeka
Faculty of Medicine
(Department of Pediatrics)
Scientific / art field,
discipline and subdiscipline		BIOMEDICINE AND HEALTHCARE
Clinical Medical Sciences
Pediatrics
Abstract (english)
Gastrointestinal pathologies are frequent in patients withtrisomy 21, but normally concerns developmental abnor-malities of the gastrointestinal tract, Hirschsprung disease orintestinal pathologies with verosimilar genetic basis, such asgluten enteropathy.1Clustering of cases of Crohn’s diseaseaccording to family, race and ethnicity, as well as increasedincidence of some human leukocyte antigens (HLA) loci inthese patients supports the role of genetic factors in thedisease.2Further indirect evidence for a genetic basis forCrohn’s disease is the reported association with Ullrich–Turner syndrome, Hermansky–Pudlak syndrome, muco-viscidosis and other disorders with known geneticetiologies.3–5Since we found only one previous report of thepresence of Crohn’s disease in a patient with trisomy 21,6wewould like to report on this extremely rare association(trisomy 21, anal atresia and Crohn’s disease) found in ourpatient.
Keywords (english)
Languageenglish
Publication typeScientific paper - Case study
Publication statusPublished
Peer reviewPeer review - international
Publication versionPublished version
Journal titlePediatrics International
Numberingvol. 43, no. 5, pp. 519-521
p-ISSN1328-8067
e-ISSN1442-200X
DOIhttps://doi.org/10.1046/j.1442-200X.2001.01431.x
URN:NBNurn:nbn:hr:184:996970
Publication2001-10-05
Document URLhttp://doi.wiley.com/10.1046/j.1442-200X.2001.01431.x
Type of resourceText
Access conditionsRestricted access
Terms of useLicence In copyright icon
Created on2023-02-01 07:41:08