TY  - JOUR
A1  - von Bernuth, Horst
A1  - Ravindran, Ethiraj
A1  - Du, Hang
A1  - Froehler, Sebastian
A1  - Strehl, Karoline
A1  - Kraemer, Nadine
A1  - Issa-Jahns, Lina
A1  - Amulic, Borko
A1  - Ninnemann, Olaf
A1  - Xiao, Mei-Sheng
A1  - Eirich, Katharina
A1  - Koelsch, Uwe
A1  - Hauptmann, Kathrin
A1  - John, Rainer
A1  - Schindler, Detlev
A1  - Wahn, Volker
A1  - Chen, Wei
A1  - Kaindl, Angela M.
T1  - Combined immunodeficiency develops with age in Immunodeficiency-centromeric instability-facial anomalies syndrome 2 (ICF2)
T2  - Orphanet Journal of Rare Dieeases
N2  - The autosomal recessive immunodeficiency-centromeric instability-facial anomalies syndrome (ICF) is characterized by immunodeficiency, developmental delay, and facial anomalies. ICF2, caused by biallelic ZBTB24 gene mutations, is acknowledged primarily as an isolated B-cell defect. Here, we extend the phenotype spectrum by describing, in particular, for the first time the development of a combined immune defect throughout the disease course as well as putative autoimmune phenomena such as granulomatous hepatitis and nephritis. We also demonstrate impaired cell-proliferation and increased cell death of immune and non-immune cells as well as data suggesting a chromosome separation defect in addition to the known chromosome condensation defect.
KW  - ZBTB24
KW  - ICF2
KW  - granulomas
KW  - facial anomalies
KW  - centromeric instability
KW  - intellectual disability
KW  - lymphoma
KW  - ZBTB24 mutations
KW  - DNMT3B
KW  - TYPE-2
KW  - immunodeficiency
KW  - microcephaly
KW  - DNA methyltransferase gene
Y1  - 2014
UR  - https://opus.bibliothek.uni-wuerzburg.de/frontdoor/index/index/docId/11485
UR  - https://nbn-resolving.org/urn:nbn:de:bvb:20-opus-114859
VL  - 9
ER  -