Cargando…
Human TYK2 deficiency: Mycobacterial and viral infections without hyper-IgE syndrome
Autosomal recessive, complete TYK2 deficiency was previously described in a patient (P1) with intracellular bacterial and viral infections and features of hyper-IgE syndrome (HIES), including atopic dermatitis, high serum IgE levels, and staphylococcal abscesses. We identified seven other TYK2-defic...
Ejemplares similares
-
A Novel Homozygous p.R1105X Mutation of the AP4E1 Gene in Twins with Hereditary Spastic Paraplegia and Mycobacterial Disease
por: Kong, Xiao-Fei, et al.
Publicado: (2013) -
ISG15: leading a double life as a secreted molecule
por: Bogunovic, Dusan, et al.
Publicado: (2013) -
Association Study of Genes Controlling IL-12-dependent IFN-γ Immunity: STAT4 Alleles Increase Risk of Pulmonary Tuberculosis in Morocco
por: Sabri, Ayoub, et al.
Publicado: (2014) -
Impaired IL-23–dependent induction of IFN-γ underlies mycobacterial disease in patients with inherited TYK2 deficiency
por: Ogishi, Masato, et al.
Publicado: (2022) -
Dual T cell– and B cell–intrinsic deficiency in humans with biallelic RLTPR mutations
por: Wang, Yi, et al.
Publicado: (2016)