دورية أكاديمية

Pure Red Cell Aplasia (PRCA) and Cerebellar Hypoplasia as Atypical Features of Polyglandular Autoimmune Syndrome Type I (APS-1): Two Sisters With the Same AIRE Mutation but Different Phenotypes

التفاصيل البيبلوغرافية
العنوان: Pure Red Cell Aplasia (PRCA) and Cerebellar Hypoplasia as Atypical Features of Polyglandular Autoimmune Syndrome Type I (APS-1): Two Sisters With the Same AIRE Mutation but Different Phenotypes
المؤلفون: Matteo Chinello, Margherita Mauro, Gaetano Cantalupo, Rita Balter, Massimiliano De Bortoli, Virginia Vitale, Ada Zaccaron, Elisa Bonetti, Rossella Gaudino, Elena Fiorini, Simone Cesaro
المصدر: Frontiers in Pediatrics, Vol 7 (2019)
بيانات النشر: Frontiers Media S.A., 2019.
سنة النشر: 2019
المجموعة: LCC:Pediatrics
مصطلحات موضوعية: polyglandular autoimmune syndrome type I, pure red cell aplasia (PRCA), hematopoietic stem cell transplantation (HCT), cerebellar hypoplasia, acute disseminated encephalomyelitis (ADEM), Pediatrics, RJ1-570
الوصف: The polyglandular autoimmune syndrome type I is a rare hereditary autosomal recessive disease. We describe a child with the classic triad of the disease and her sister with pure red cell aplasia and cerebellar hypoplasia. The latter received two haematopoietic stem cell transplantations, complicated by an acute disseminated encephalomyelitis.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 2296-2360
العلاقة: https://www.frontiersin.org/article/10.3389/fped.2019.00051/fullTest; https://doaj.org/toc/2296-2360Test
DOI: 10.3389/fped.2019.00051
الوصول الحر: https://doaj.org/article/74534a58c2b748a08db2b75c6c8d21caTest
رقم الانضمام: edsdoj.74534a58c2b748a08db2b75c6c8d21ca
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:22962360
DOI:10.3389/fped.2019.00051