Bu öğeden alıntı yapmak, öğeye bağlanmak için bu tanımlayıcıyı kullanınız:
http://hdl.handle.net/11452/28191
Başlık: | Orf infection in a patient with stat1 gain-of-function |
Yazarlar: | Puel, Anne Casanova, Jean-Laurent Uludağ Üniversitesi/Tıp Fakültesi/Dahili Tıp Bilimleri Bölümü/Çocuk Sağlığı ve Hastalıkları Anabilim Dalı. 0000-0001-8571-2581 Kılıç, Sara Şebnem AAH-1658-2021 34975059200 |
Anahtar kelimeler: | Chronic Mucocutaneous Candidiasis Orf infection STAT1 gain-of-function Primary immunodeficiency Immunology Virus infection Giant orf Immunity Autoantibodies Deficiency Mutations Lymphoma Humans Il-17a |
Yayın Tarihi: | Oca-2015 |
Yayıncı: | Springer/Plenum Publishers |
Atıf: | Kılıç, S. Ş. vd. (2015). "Orf infection in a patient with stat1 gain-of-function". Journal of Clinical Immunology, 35(1), 80-83. |
Özet: | Chronic Mucocutaneous Candidiasis (CMC) refers to a group of immunodeficiencies, characterized by persistent or recurrent infections of the skin, nails, and mucosae caused by Candida. It is typically caused by inborn errors of IL-17 immunity. Orf, also known as contagious ecthyma, is a zoonotic infection caused by a dermatotropic parapoxvirus that commonly infects sheep and goats; it is transmitted to humans through contact with an infected animal or fomites. While orf is usually a benign self-limiting illness, it can be progressive and even life-threatening in immune-compromised hosts. A 34-year-old man with autosomal dominant CMC due to a heterozygous STAT1 gain-of-function (GOF) mutation cut his hand with a knife during slaughter. Giant orf infection developed in 2 weeks. He was successfully treated by cidofovir injections every other week for 4 months. This is the first patient with severe orf in the context of a well-defined genetically identified PID: CMC and inborn error of IL-17 immunity due to a GOF STAT1 mutation. |
URI: | https://doi.org/10.1007/s10875-014-0111-7 https://link.springer.com/article/10.1007/s10875-014-0111-7 http://hdl.handle.net/11452/28191 |
ISSN: | 0271-9142 1573-2592 |
Koleksiyonlarda Görünür: | PubMed Scopus Web of Science |
Bu öğenin dosyaları:
Bu öğeyle ilişkili dosya bulunmamaktadır.
DSpace'deki bütün öğeler, aksi belirtilmedikçe, tüm hakları saklı tutulmak şartıyla telif hakkı ile korunmaktadır.