نتایج جستجو برای: alport syndrome

تعداد نتایج: 622022  

2012
Thais Z. igami WalTer Y. Takahashi YoshiTaka nakashima

In 1927, Alport described the association of hereditary nephritis with sensorineural deafness observed in a family. In 1954, Sohar des­ cribed the presence of crystalline lens malformation associated with renal and hearing impairment. Finally, in 1961, Julien Marie reported the binding of Alport syndrome (AS) in the presence of anterior len­ ticonus. As occurs in an approximate incidence of 1 f...

2009
Young-Sil An Deog-Yoon Kim

Diffuse esophageal leiomyomatosis is a rare benign tumor, which can be associated with leiomyoma in female genital tracts involving the uterus, vagina, and vulva. Alport syndrome, an inherited disorder that includes the kidneys, eyes, and sensorineural hearing loss, is also rarely associated with these multiple leiomyomatosis. In our case, (18)F-fluorodeoxyglucose positron emission tomography/c...

رحیم‌زاده, ناهید, اتوکش, حسن , اداباقری, زهرا ,

ABSTRACT The various types of Glomerolunephritis (from the point of view of pathology) have different clinical and para-clinical presentations. Knowledge of such symptoms in each pathology could be very helpful in determining correct and precise clinical diagnosis. Therefore we decided to indicate all the clinical and para-clinical symptoms in 280 cases of biopsy and on the other ha...

2011
Lobna Ayadi Karima Abbes Saloua Makni Mahmoud Kharrat Rim Kallel Najmeddine Affes Mohamed Ben Hmida Jamil Hachicha Mohamed Issam Beyrouti Tahya Sellami Boudawara

Note Alport Syndrome (AS) is a rare hereditary glomerular nephropathy, its incidence is approximatively 1/5000 individuals. Its association with leiomyomatosis is estimated at 5% of the cases. Leiomyomatosis tends to affect young boys (mean age: 6 years) and women at a mean age of 40 years. In contrast to the renal lesions which are less severe among women, the leiomyomatosis is as severe in wo...

Journal: :Nephrology Dialysis Transplantation 2016

Journal: :Journal of the American Society of Nephrology 1998

2006
Karl Tryggvason Jaakko Patrakka

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...

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