Academic Journal
Birt Hogg Dube sendromu: Nadir görülen ailesel akciğer hastalığı [Birt Hogg Dube syndrome: Rare family lung disease]
العنوان: | Birt Hogg Dube sendromu: Nadir görülen ailesel akciğer hastalığı [Birt Hogg Dube syndrome: Rare family lung disease] |
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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 |
تدمد: | 33853312 04941373 |
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DOI: | 10.5578/tt.20219913 |