Academic Journal

Birt Hogg Dube sendromu: Nadir görülen ailesel akciğer hastalığı [Birt Hogg Dube syndrome: Rare family lung disease]

التفاصيل البيبلوغرافية
العنوان: Birt Hogg Dube sendromu: Nadir görülen ailesel akciğer hastalığı [Birt Hogg Dube syndrome: Rare family lung disease]
المؤلفون: Şimşek ŞM., Savaş R., Temiz P., Çelik P.
بيانات النشر: NLM (Medline)
سنة النشر: 2021
المجموعة: Ege University Institutional Repository
الوصف: Birt Hogg Dube syndrome is a rare disease characterized by autosomal dominant inherited multiple cysts in the lungs, renal tumors and skin fibrofolliculomas. It was first described in 1977 by Birt et al. In this case report, a patient who was diagnosed with symptoms and his first degree relative is presented. Diseases that should be considered in differential diagnosis are discussed. The diagnosis of this disease is usually made after recurrent pneumothorax. Since it is a genetic disease, the importance of follow-up and screening needs of patients and their relatives is emphasized.
نوع الوثيقة: article in journal/newspaper
اللغة: English
تدمد: 33853312
0494-1373
Relation: Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı; Tuberkuloz ve toraks; https://doi.org/10.5578/tt.20219913; https://hdl.handle.net/11454/71471; 69; 102; 106
DOI: 10.5578/tt.20219913
الاتاحة: https://hdl.handle.net/11454/71471
https://doi.org/10.5578/tt.20219913
Rights: open
رقم الانضمام: edsbas.D27A0461
قاعدة البيانات: BASE
الوصف
تدمد:33853312
04941373
DOI:10.5578/tt.20219913