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akaturk Akademik ölçüm

Makale detayı · 2017 · article

title Gain-of-Function Mutations in iSTAT1/i : A Recently Defined Cause for Chronic Mucocutaneous Candidiasis Disease Mimicking Combined Immunodeficiencies/title

ISSN2090-6609
YÖKSİS OpenAlex Açık erişim · gold
Yıl2017
Atıf39OpenAlex
Yüzdelik%81,9
FWCI1,511,00 = dünya ortalaması
Scopus (SJR)Q4

Veri kaynağı ayrımı

  • YÖKSİSYÖKSİS makale kaydı
  • YÖKSİS dergi adıCase Reports in Immunology
  • Katalog eşleşmesi (ISSN)Case Reports in Immunology
  • OpenAlexOpenAlex zenginleştirmesi (özet, atıf, konular)
  • Semantic Scholaratıf sayısı (OpenAlex ile birleştirilmez)

Özet

OpenAlex İngilizce

Chronic Mucocutaneous Candidiasis (CMC) is the chronic, recurrent, noninvasive Candida infections of the skin, mucous membranes, and nails. A 26-month-old girl was admitted with the complaints of recurrent oral Candidiasis, diarrhea, and respiratory infections.Candida albicansgrew in oral mucosa swab. CMV and EBV DNA titers were elevated. She had hypergammaglobulinemia; IgE level, percentages of lymphocyte subgroups, and in vitro T-cell proliferation responses were normal. She had parenchymal nodules within the lungs and a calcific nodule in the liver. Chronic-recurrent infections with different pathogens leading to significant morbidity suggested combined immunodeficiency, CMC, or Mendelian susceptibility to mycobacterial diseases. Genetic analysis revealed a predefined heterozygous gain-of-function mutation (GOF) (c.1154 C>T, p.Thr385Met) in the gene coding STAT1 molecule. Hematopoietic stem cell transplantation (HSCT) was planned because of severe recurring infections. Patients withSTAT1GOF mutations may exhibit diverse phenotypes including infectious and noninfectious findings. HSCT should be considered as an early treatment option before permanent organ damage leading to morbidity and mortality develops. This case is presented to prompt clinicians to considerSTAT1GOF mutations in the differential diagnosis of patients with chronic Candidiasis and recurrent infections with multiple organisms, since these mutations are responsible for nearly half of CMC cases reported.

Konular

Atıflar

OpenAlex cited_by_count. WoS veya Scopus atıf sayısı değildir; o kaynaklar için ayrı kolon yoktur.

39atıfOpenAlex · cited_by_count (önbellek / veritabanı)

Yerel katalogda bu makaleye atıf yapan 6 yayın (OpenAlex referans eşleşmesi; tam dünya listesi değildir).

  1. 2024 Current genetic defects in common variable immunodeficiency patients on the geography between Europe and Asia: a single-center experienceAtıf 5 · OpenAlex
  2. 2024 Current genetic defects in common variable immunodeficiency patients on the geography between Europe and Asia: a single-center experienceAtıf 5 · OpenAlex
  3. 2024 Current genetic defects in common variable immunodeficiency patients on the geography between Europe and Asia: a single-center experienceAtıf 5 · OpenAlex
  4. 2024 Current genetic defects in common variable immunodeficiency patients on the geography between Europe and Asia: a single-center experienceAtıf 5 · OpenAlex
  5. 2024 Current genetic defects in common variable immunodeficiency patients on the geography between Europe and Asia: a single-center experienceAtıf 5 · OpenAlex
  6. 2023 Current genetic defects in common variable immunodeficiency patients on the geography between Europe and Asia: a single-center experienceAtıf 5 · OpenAlex

Yazarlar

9
  1. sanem akarcan 1
  2. ulusoy ezgi 2
  3. NESLİHAN KARACA EGE ÜNİVERSİTESİ 3
  4. oşık esra 4
  5. aksu guzide 5
  6. ferda evin 6
  7. azarsiz elif 7
  8. ouel anne 8
  9. kutukçuler necil 9