The Many Faces of Thin Basement Membrane Nephropathy; A Population Based Study

نویسندگان

  • Kyriacos Kyriacou
  • Ioanna Zouvani
  • Christina Flouri
  • Maria Loizidou
  • Michael Hadjigavriel
  • Andreas Hadjisavvas
  • Kyriacos Ioannou
چکیده

Thin basement membrane nephropathy (TBMN) or benign familial hematuria, is one of the commonest kidney disorders, characterized by recurrent benign hematuria, which is often associated with a family history (Gregory, 2005). It is generally considered to be a nonprogressive, life long disorder with a rather benign course (Tryggvason & Patrakka, 2006), although data from some studies show that a proportion of patients manifest more severe symptoms, than originally described and eventually develop endstage renal disease (ESRD) (Dische, Weston, & Parsons, 1985; Frasca et al., 2005; Pierides et al., 2009; Tiebosch et al., 1989). TBMN was first described in 1926 (Baer, 1926) and at presentation is usually characterized by microscopic painless hematuria, by little or negligible proteinuria and normal renal function. TBMN is an autosomal dominant disorder and more than 50% of the cases have a family history of hematuria. In about 40% of families with a confirmed diagnosis of TBMN the condition co-segregates with heterozygous COL4A3/COL4A4 mutations (Lemmink et al., 1996). Mutations in the type IV collagen gene family which also includes the COL4A5 gene, also cause Alport syndrome (Hostikka et al., 1990). It is believed that these disorders are the result of defective, synthesis and/or assembly, of the critical glycoprotein components, that form the glomerular basement membranes (GBMs), among which type IV collagen, is the major constituent. Clinically TBMN must be differentially diagnosed, between IgA nephropathy and Alport syndrome which are the other two main causes of hematuria, particularly in children. The need for differential diagnosis, often necessitates the examination of a kidney biopsy at the electron microscopical level, which also enables measurement of the thickness of the GBMs. Indeed Rogers et al (Rogers, Kurtzman, Bunn, & White, 1973) were the first to associate recurrent benign hematuria with the presence of thin GBMs. Currently the most widely

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Disease of the Month Thin Basement Membrane Nephropathy

T hin basement membrane nephropathy (TBMN) is the most common cause of persistent hematuria in children and adults, the other main causes being IgA nephropathy and Alport syndrome (1–3). In addition to hematuria, patients with TBMN usually have minimal proteinuria, normal renal function, and uniformly thinned glomerular basement membranes (GBM), as determined by electron microscopy. TBMN, which...

متن کامل

IgA nephropathy combined with thin basement membrane nephropathy in children

IgA Nephropathy (IgAN) and thin basement membrane nephropathy (TBMN) are the most common and important causes of persistent hematuria in childhood, and with great interest I have read the published article by Hwang et al [1] that appeared in a recent issue of Kidney Research and Clinical Practice entitled “Clinical manifestations of IgA nephropathy combined with thin glomerular basement membran...

متن کامل

The clinical features of thin basement membrane nephropathy.

Thin basement membrane nephropathy (TBMN) is a common, lifelong condition affecting the kidneys that is characterized by microscopic glomerular hematuria, minimal or no proteinuria, and normal renal function. It often is discovered incidentally, and usually has an excellent prognosis. Many cases are familial and show autosomal-dominant inheritance. The defining characteristic is a glomerular ba...

متن کامل

Thin basement membrane nephropathy associated with other glomerular diseases.

Many reports confirm that thin basement membrane nephropathy (TBMN) commonly occurs together with other glomerular diseases such as minimal change glomerulonephritis, diabetes, membranous nephropathy, immunoglobulin (Ig)A glomerulonephritis, and focal segmental glomerulosclerosis. We postulate 3 explanations for these observations. The association of minimal change glomerulonephritis with TBMN ...

متن کامل

Impact of gene polymorphisms of interleukin-18, transforming growth factor-β, and vascular endothelial growth factor on development of IgA nephropathy and thin glomerular basement membrane disease.

BACKGROUND We investigated the effects of gene polymorphisms on the development of IgA nephropathy and thin glomerular basement membrane (GBM) disease by analyzing polymorphisms in the interleukin (IL)-18, transforming growth factor (TGF)-β, and vascular endothelial growth factor (VEGF) genes in Korean patients. METHODS This study included 146 normal individuals and 69 biopsy-proven IgA nephr...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

عنوان ژورنال:

دوره   شماره 

صفحات  -

تاریخ انتشار 2017