Skeletal Manifestations in Gaucher Disease: A Case Report

• প্রধান লেখক: Altınay Göksel Karatepe (লেখক), Rezzan Günaydın (লেখক), Taciser Kaya (লেখক), Nesrin Şen (লেখক), Gülriz Özbek (লেখক), Özgür Sipahi Esen (লেখক)
• বিন্যাস: গ্রন্থ
• প্রকাশিত: Galenos Yayinevi, 2005-09-01T00:00:00Z.
• বিষয়গুলি: article
• অনলাইন ব্যবহার করুন: Connect to this object online.

Gauchers disease is the most frequent hereditary lysosomal deposit storage disorder. It is characterized by a deficiency of the enzyme glucocerebrosidase that leads to an accumulation of glucocerebroside in the macrophage lysosomes. It is classified in three types, according to the presence of centr...