Down syndrome and Crohn's disease: An extremely rare association

Pediatrics International

Volumn 43, Issue 5, 2001, Pages 519-521

  Persic, Mladen ^a   Dessardo, Sandro ^a,b   Subat Dezulović, Mirna ^a   Ahel, Vladimir ^a   Rožmanić, Vojko ^a  

^a UNIVERSITY OF RIJEKA   (Croatia)

^b Clinical Hospital Centre Rijeka Children's Hospital Kantrida   (Croatia)

Author keywords

Anal atresia; Crohn's disease; Down syndrome; Genetics

Indexed keywords

AZATHIOPRINE; PREDNISONE; SALAZOSULFAPYRIDINE;

ARTICLE; CASE REPORT; CLINICAL FEATURE; COLONOSCOPY; CROHN DISEASE; CYSTOCOLIC FISTULA; DISEASE ASSOCIATION; DOWN SYNDROME; FEMALE; FOLLOW UP; HISTOPATHOLOGY; HUMAN; LABORATORY TEST; PHYSICAL EXAMINATION; PRIORITY JOURNAL;

CHILD; CROHN DISEASE; DOWN SYNDROME; FEMALE; HUMANS; INTESTINAL FISTULA; SULFASALAZINE; URINARY BLADDER FISTULA;

EID: 0035725140     PISSN: 13288067     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1442-200X.2001.01431.x     Document Type: Article

References (9)

1. Down syndrome and the gastrointestinal tract
2. Genetic markers may predict disease behavior in patients with ulcerative colitis
3. A genowide analysis provides evidence for novel linkages in IBD in a large European cohort
4. Genetic defects and clinical characteristics of patients with a form of oculocutaneous albinism (Hermansky-Pudlak syndrome)
5. Unusual colitides
6. Regional enteritis and down syndrome
7. Development and validation of a paediatric Crohn's disease activity index
8. Mapping of a susceptibility focus for Crohn's disease on chromosome 16
9. Two stage genome-wide search in inflammatory bowel disease: Evidence for susceptibility loci on chromosomes 3, 7 and 12