Delayed Diagnosis of X-linked Lymphoproliferative Syndrome Type 2 in a 17-year-old Male With Severe Crohn's Disease and Recurrent Skin Infections.
XIAP deficiency
hematopoietic stem cell transplantation
primary immunodeficiency disease
Journal
JPGN reports
ISSN: 2691-171X
Titre abrégé: JPGN Rep
Pays: United States
ID NLM: 101773885
Informations de publication
Date de publication:
Aug 2021
Aug 2021
Historique:
received:
18
12
2020
accepted:
02
06
2021
medline:
12
7
2021
pubmed:
12
7
2021
entrez:
19
5
2023
Statut:
epublish
Résumé
X-linked lymphoproliferative syndrome type 2 (XLP2) is a rare genetic primary immunodeficiency disease caused by mutations in the
Identifiants
pubmed: 37205951
doi: 10.1097/PG9.0000000000000102
pmc: PMC10191492
doi:
Types de publication
Case Reports
Langues
eng
Pagination
e102Informations de copyright
Copyright © 2021 The Author(s). Published by Wolters Kluwer on behalf of European Society for Pediatric Gastroenterology, Hepatology, and Nutrition and North American Society for Pediatric Gastroenterology, Hepatology, and Nutrition.
Déclaration de conflit d'intérêts
The authors report no funding and conflicts of interest.
Références
J Pediatr Gastroenterol Nutr. 2019 Jul;69(1):e13-e18
pubmed: 31232887
J Clin Immunol. 2018 Apr;38(3):330-444
pubmed: 29682684
Inflamm Bowel Dis. 2020 Apr 11;26(5):720-727
pubmed: 31375816
J Clin Immunol. 2017 Jan;37(1):85-91
pubmed: 27815752
J Clin Immunol. 2017 Jan;37(1):67-79
pubmed: 27747465
J Allergy Clin Immunol. 2014 Nov;134(5):1131-41.e9
pubmed: 24942515
Gastroenterology. 2020 Jun;158(8):2208-2220
pubmed: 32084423
J Clin Immunol. 2015 May;35(4):331-8
pubmed: 25737324
World J Gastroenterol. 2018 Mar 7;24(9):1035-1045
pubmed: 29531467
Gastroenterology. 2018 Jun;154(8):2165-2177
pubmed: 29501442