Gaucher Hastalığı (Olgu Sunumu)
Küçük Resim Yok
Tarih
2001
Dergi Başlığı
Dergi ISSN
Cilt Başlığı
Yayıncı
Erişim Hakkı
info:eu-repo/semantics/closedAccess
Özet
Gaucher disease is a rarely seen autosomal recessive disorder associated with enzyme defect. Most commonly seen among Ashkenazian Jewish and its incidence in U.S.A is between 1110.000-20.0000. Our case is a female patient of 25 years old admitted with the diagnosis of hypersplenism. On investigating of Gaucher cells seen in the bone marrow, the diagnosis of Type I Gaucher disease is obtained. Splenectomy has been done. Hematological values returned to normal levels on the 5th. postoperative day. The case was presented because of its rarity and its clinical improvement after splenectomy.
Açıklama
Anahtar Kelimeler
Cerrahi
Kaynak
Çağdaş Cerrahi Dergisi
WoS Q Değeri
Scopus Q Değeri
Cilt
15
Sayı
1
Künye
Aksoy, F., Vatansev, C., Borazan, A., Bilgiçli, N., (2001). Gaucher Hastalığı (Olgu Sunumu). Çağdaş Cerrahi Dergisi, 15(1), 61-62.
