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akaturk Akademik ölçüm

Makale detayı · 2021

Birt Hogg Dube syndrome: Rare family lung disease

Tuberk Toraks

YÖKSİS OpenAlex Açık erişim · diamond SJR Q3 TR Index Atıf 0 Yüzdelik 5.5% FWCI 0.0
Yıl
2021
ISSN
0494-1373
Tür
article

Veri kaynağı ayrımı

  • YÖKSİS YÖKSİS makale kaydı
  • OpenAlex OpenAlex zenginleştirmesi (özet, atıf, konular)

Özet

İngilizce (OpenAlex)

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.

Konular

  • Renal cell carcinoma treatment
  • Genetic and Kidney Cyst Diseases
  • Medical Imaging and Pathology Studies

Birincil konu Renal cell carcinoma treatment

Yazarlar

  1. ŞABAN MELİH ŞİMŞEK GİRESUN ÜNİVERSİTESİ
  2. RECEP SAVAŞ EGE ÜNİVERSİTESİ
  3. PEYKER TEMİZ
  4. PINAR ÇELİK MANİSA CELÂL BAYAR ÜNİVERSİTESİ