Zobrazeno 1 - 10
of 781
pro vyhledávání: '"Very early onset"'
Autor:
Anatoly I. Khavkin, Anastasiya A. Permyakova, Mariya O. Tsepilova, Aleksandra V. Kaplina, Stanislav I. Sitkin, Andrey N. Surkov, Stanislav D. Getmanov
Publikováno v:
Вопросы современной педиатрии, Vol 23, Iss 3, Pp 145-151 (2024)
Nowadays, an urgent problem of pediatric gastroenterology is the study of inflammatory bowel diseases with very early onset (VEO-IBD), which have unique genetic, clinical, immunological, morphological, and laboratory sings. Early VEO-IBD is usually c
Externí odkaz:
https://doaj.org/article/842641a971ca452f885777c08f4d0908
Publikováno v:
BMC Medical Genomics, Vol 17, Iss 1, Pp 1-7 (2024)
Abstract Background With recent advances in gene sequencing technology, more than 60 genetic mutations associated with very early onset inflammatory bowel disease (VEO-IBD) have been reported. Most of the genes are associated with immune deficiencies
Externí odkaz:
https://doaj.org/article/f18f833ad5ff4d368a129785dd72d533
Autor:
Afif Alshwaiki, Ranim M. H. D. Samir Nakhal, Ali Alakbar Nahle, Hussein Hamdar, Nafiza Martini, Jaber Mahmod
Publikováno v:
Journal of Medical Case Reports, Vol 18, Iss 1, Pp 1-6 (2024)
Abstract Background Inflammatory bowel diseases, consisting of Crohn’s disease and ulcerative colitis, are chronic bowel relapsing inflammatory disorders. Inflammatory bowel diseases begin rarely in infants. Approximately 25% of patients with infla
Externí odkaz:
https://doaj.org/article/dc46e7889ef546508d680dfd8a7f739b
Autor:
Máire A. Conrad, Kyle Bittinger, Yue Ren, Kelly Kachelries, Jennifer Vales, Hongzhe Li, Gary D. Wu, Frederic D. Bushman, Marcella Devoto, Robert N Baldassano, Judith R. Kelsen
Publikováno v:
Gut Microbes, Vol 16, Iss 1 (2024)
ABSTRACTDysbiosis is associated with pediatric and adult-onset inflammatory bowel disease (IBD), but the role of dysbiosis and the microbiome in very early onset IBD (VEO-IBD) has not yet been described. Here, we aimed to demonstrate the impact of ag
Externí odkaz:
https://doaj.org/article/75bceb6e38a04628a5628960e23be4f7
Autor:
Yohei Taniguchi, Kenichiro Miura, Yoko Shira, Takuya Fujimaru, Eisei Sohara, Yutaka Yamaguchi, Motoshi Hattori
Publikováno v:
Kidney Medicine, Vol 6, Iss 8, Pp 100857- (2024)
Recent studies have described several children with very early-onset polycystic kidney disease (PKD) that mimicked autosomal recessive polycystic kidney disease because of 2 hypomorphic PKD1 gene variants. However, no reports have described pathologi
Externí odkaz:
https://doaj.org/article/49fffedab7a34e8f86a40d4e320eafb9
Autor:
Lorraine Stallard, Karen Frost, Nathaniel Frost, Luca Scarallo, Eric I. Benchimol, Thomas D. Walters, Peter C. Church, Anne M. Griffiths, Aleixo M. Muise, Amanda Ricciuto
Publikováno v:
Gastro Hep Advances, Vol 3, Iss 2, Pp 215-220 (2024)
Background and Aims: Children with very early onset inflammatory bowel disease (VEO-IBD) are uniquely at risk of inadequate infliximab (IFX) exposure. We studied the association between standard body weight (BW)-based and body surface area (BSA)-base
Externí odkaz:
https://doaj.org/article/3eb6c20325164b7f9a5775d5201e6f3e
Publikováno v:
Frontiers in Neurology, Vol 15 (2024)
Pediatric onset multiple sclerosis (POMS) in the very young is a very rare entity and presents a difficult diagnostic challenge due to overlapping signs and symptoms with other diseases. We present a 4-year-old boy who initially presented with right-
Externí odkaz:
https://doaj.org/article/4531950745e3492c9eec170c4e48c326
Publikováno v:
BMC Gastroenterology, Vol 23, Iss 1, Pp 1-7 (2023)
Abstract Background Very early-onset inflammatory bowel disease (VEOIBD) with interleukin-10 (IL10R) signaling deficiency usually requires enterostomy in patients who are refractory to traditional treatment. This study aimed to evaluate long-term out
Externí odkaz:
https://doaj.org/article/76cf1caaffa0451e9cda948edfcc6aa1
Autor:
Margaret Irwin, Veeraya K. Tanawattanacharoen, Amy Turner, Mary Beth F. Son, Rebecca C. Hale, Craig D. Platt, Juan Putra, Birgitta A.R. Schmidt, Mollie G. Wasserman
Publikováno v:
Pediatric Rheumatology Online Journal, Vol 21, Iss 1, Pp 1-5 (2023)
Abstract Background Sweet syndrome (SS), also known as acute febrile neutrophilic dermatosis, is an immunologic syndrome characterized by widespread neutrophilic infiltration. Histiocytoid Sweet syndrome (H-SS) is a histopathologic variant of SS. Whi
Externí odkaz:
https://doaj.org/article/dd0cf0f729d34e20b4b04ea44e1763df
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