prikaz prve stranice dokumenta Down syndrome and Crohn’s disease: An extremely rare association
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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. i 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, br. 5, 2001, str. 519-521. https://doi.org/10.1046/j.1442-200X.2001.01431.x

Peršić, Mladen, Sandro Dessardo, Mirna Šubat Dežulović, Vladimir Ahel i Vojko Rožmanić. "Down syndrome and Crohn’s disease: An extremely rare association." Pediatrics International 43, br. 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), str. 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]. 05.10.2001. [pristupljeno 12.11.2024.];43(5):519-521. doi: 10.1046/j.1442-200X.2001.01431.x

M. Peršić, S. Dessardo, M. Šubat Dežulović, V. Ahel i V. Rožmanić, "Down syndrome and Crohn’s disease: An extremely rare association", Pediatrics International, vol. 43, br. 5, str. 519-521, Listopad 2001. [Online]. Dostupno na: https://urn.nsk.hr/urn:nbn:hr:184:996970. [Citirano: 12.11.2024.]

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Podaci o radu
Naslov (engleski)Down syndrome and Crohn’s disease: An extremely rare association
AutorMladen Peršić
AutorSandro Dessardo
AutorMirna Šubat-Dežulović
AutorVladimir Ahel
AutorVojko Rožmanić
Autorova ustanovaSveučilište u Rijeci
Medicinski fakultet
(Katedra za pedijatriju)
Znanstveno / umjetničko
područje, polje i grana		BIOMEDICINA I ZDRAVSTVO
Kliničke medicinske znanosti
Pedijatrija
Sažetak (engleski)
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.
Ključne riječi (engleski)
Jezikengleski
Vrsta publikacijeZnanstveni rad - Prikaz slučaja
Status objaveObjavljen
Vrsta recenzijeRecenziran - međunarodna recenzija
Verzija publikacijeObjavljena verzija rada (izdavačev PDF)
Naslov časopisaPediatrics International
Brojčani podacivol. 43, br. 5, str. 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
Datum objave publikacije2001-10-05
URL dokumentahttp://doi.wiley.com/10.1046/j.1442-200X.2001.01431.x
Vrsta resursaTekst
Prava pristupaOgraničen pristup
Uvjeti korištenjaIkona licence Zaštićeno autorskim pravom.
Datum i vrijeme pohrane2023-02-01 07:41:08