Atıf İçin Kopyala
Berberoglu-Ates B., VARAN A., DEMİR H., AKYÜZ C., YÜCE A.
TURKISH JOURNAL OF PEDIATRICS, cilt.61, sa.3, ss.449-452, 2019 (SCI-Expanded)
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Yayın Türü:
Makale / Tam Makale
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Cilt numarası:
61
Sayı:
3
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Basım Tarihi:
2019
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Doi Numarası:
10.24953/turkjped.2019.03.022
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Dergi Adı:
TURKISH JOURNAL OF PEDIATRICS
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Derginin Tarandığı İndeksler:
Science Citation Index Expanded (SCI-EXPANDED), Scopus, TR DİZİN (ULAKBİM)
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Sayfa Sayıları:
ss.449-452
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Hacettepe Üniversitesi Adresli:
Evet
Özet
Gaucher disease (GD) is the most prevalant lysosomal lipid storage disease that results from loss of function of acid beta-glucosidase due to mutations in the glucocerebrosidase gene. Common features of all types of GD include hepatosplenomegaly, cytopenia, and various patterns of bone and lung involvement.