کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
3852338 | 1598382 | 2006 | 5 صفحه PDF | دانلود رایگان |
عنوان انگلیسی مقاله ISI
Hereditary Periodic Fever With Systemic Amyloidosis: Is Hyper-IgD Syndrome Really a Benign Disease?
دانلود مقاله + سفارش ترجمه
دانلود مقاله ISI انگلیسی
رایگان برای ایرانیان
کلمات کلیدی
موضوعات مرتبط
علوم پزشکی و سلامت
پزشکی و دندانپزشکی
بیماریهای کلیوی
پیش نمایش صفحه اول مقاله
![عکس صفحه اول مقاله: Hereditary Periodic Fever With Systemic Amyloidosis: Is Hyper-IgD Syndrome Really a Benign Disease? Hereditary Periodic Fever With Systemic Amyloidosis: Is Hyper-IgD Syndrome Really a Benign Disease?](/preview/png/3852338.png)
چکیده انگلیسی
We report a case of amyloidosis in association with hyperimmunoglobulinemia D syndrome (HIDS). The patient showed typical clinical features of HIDS. He had crescentic glomerulonephritis progressing to end-stage renal disease at age 13 years. Eight years later, he developed an AA-type amyloidosis with extensive involvement of the intestine, respiratory tract, and thyroid gland. These unusual complications of HIDS seriously challenge the assumption that the disease is associated with a good prognosis.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: American Journal of Kidney Diseases - Volume 48, Issue 3, September 2006, Pages e41-e45
Journal: American Journal of Kidney Diseases - Volume 48, Issue 3, September 2006, Pages e41-e45
نویسندگان
Rainer MD, Jörg MD, PhD, Rolf Dieter MD, PhD, Christof MD, PhD, Peter Julius MD, PhD, Christian MD,