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
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
(2019)
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
Anno:
2019
Tipologia prodotto:
Articolo in Rivista
Tipologia ANVUR:
Articolo su rivista
Lingua:
Inglese
Referee:
No
Nome rivista:
FRONTIERS IN PEDIATRICS
ISSN Rivista:
2296-2360
N° Volume:
7
Intervallo pagine:
1-7
Parole chiave:
acute disseminated encephalomyelitis (ADEM); cerebellar hypoplasia; hematopoietic stem cell transplantation (HCT); polyglandular autoimmune syndrome type I; pure red cell aplasia (PRCA)
Breve descrizione dei contenuti:
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.
Note:
The page range is based on PDF file available on the journal website
Id prodotto:
109254
Handle IRIS:
11562/997277
ultima modifica:
1 dicembre 2022
Citazione bibliografica:
Chinello, Matteo; Mauro, Margherita; Cantalupo, Gaetano; Balter, Rita; De Bortoli, Massimiliano; Vitale, Virginia; Zaccaron, Ada; Bonetti, Elisa; Gaudino, Rossella; Fiorini, Elena; Cesaro, Simone,
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«FRONTIERS IN PEDIATRICS»
, vol. 7
, 2019
, pp. 1-7