| Literature DB >> 25805655 |
H Haluk Akar1, Turkan Patiroglu2, Basak N Akyildiz3, Nazan U Tekerek3, M Sait Doğan4, Selim Doğanay4, Mirjam van der Burg5, Ruhan Dusunsel6.
Abstract
Zeta-chain associated protein 70 kDa deficiency (ZAP70) is a form of severe combined immunodeficiency (SCID). It is caused by defects in the signaling pathways associated with T-lymphocyte activation. ZAP70 deficiency is characterized by a marked reduction in peripheral CD8+ T-cells. In this report, we described two patients with ZAP70 deficiency who presented with recurrent infections, lung tuberculosis (TBC), congenital nephrotic syndrome (CNS), and silent brain infarcts (SBIs) as a common feature. The first patient initially presented with recurrent infections and TBC as in a classic SCID patient. At the age of 4, he was interned with febrile seizure. Cranial magnetic resonance imaging (MRI) showed SBIs. The second patient, an 8-month-old boy, presented with congenital nephrotic syndrome caused by cytomegalovirus (CMV) and he had also SBIs.Entities:
Keywords: Congenital nephrotic syndrome; Silent brain infarcts; ZAP70 deficiency
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Year: 2015 PMID: 25805655 DOI: 10.1016/j.clim.2015.03.014
Source DB: PubMed Journal: Clin Immunol ISSN: 1521-6616 Impact factor: 3.969