Delayed Diagnosis of X-linked Lymphoproliferative Syndrome Type 2 in a 17-year-old Male With Severe Crohn’s Disease and Recurrent Skin Infections

X-linked lymphoproliferative syndrome type 2 (XLP2) is a rare genetic primary immunodeficiency disease caused by mutations in the XIAP gene that lead to deficiency of the X-linked inhibitor of apoptosis protein. XLP2 is characterized by dysregulated immune responses and can result in an inflammatory...

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Detalles Bibliográficos
Autores principales: Zacharias, Stephanie A., Seshadri, Priyanka, Hwang, Sharon, Baker, Laura, Powell, Jonathan, Fernando del Rosario, J., Molle-Rios, Zarela
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins, Inc. 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10191492/
https://www.ncbi.nlm.nih.gov/pubmed/37205951
http://dx.doi.org/10.1097/PG9.0000000000000102

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10191492/
https://www.ncbi.nlm.nih.gov/pubmed/37205951
http://dx.doi.org/10.1097/PG9.0000000000000102

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