Alport�s Syndrome and Related Hereditary Nephropathies

2015 ◽  
pp. 82-90 ◽  
Author(s):  
Jean-Pierre Gr�nfeld ◽  
Robert Charbonneau ◽  
Gilles Grateau ◽  
Laure-H�l�ne No�l
Keyword(s):  
Hereditary Nephropathies

Exome Sequencing and Identification of Phenocopies in Patients With Clinically Presumed Hereditary Nephropathies

2020 ◽  
Vol 76 (4) ◽  
pp. 460-470 ◽  
Author(s):  
Korbinian M. Riedhammer ◽  
Matthias C. Braunisch ◽  
Roman Günthner ◽  
Matias Wagner ◽  
Clara Hemmer ◽  
...  
Keyword(s):  
Exome Sequencing ◽  
Hereditary Nephropathies

scholarly journals Сhronic kidney disease in children: principles of ambulatory management

2021 ◽  
Vol 24 (2) ◽  
pp. 122-129
Author(s):  
Albina A. Vyalkova ◽  
Svetlana A. Chesnokova ◽  
Oksana O. Ustinova ◽  
Larisa A. Gaikova
Keyword(s):  
Risk Factors ◽  
Kidney Disease ◽  
Early Diagnosis ◽  
Congenital Malformations ◽  
Urinary System ◽  
Renal Lesions ◽  
Primary Health ◽  
Uremic Syndrome ◽  
Renal Infection ◽  
Hereditary Nephropathies

Introduction. The term «chronic kidney disease» (CKD) is used to define the outcomes of various forms of chronic progressive kidney disease, characterized by kidney damage, or a decrease in their function for three months or more, regardless of the nosological diagnosis. The aim of the work was to determine the frequency, structure, and clinical and paraclinical features of CKD in children to substantiate the principles of its management in primary health care. Results. In CKD patients, tubulointerstitial renal lesions were established to prevail (80%). Associated with congenital malformations of the urinary system, reflux uropathy, and urolithiasis in 98% of cases tubulointerstitial renal lesions are complicated by renal infection. In 8.9% of children, CKD was formed as an outcome of glomerulopathies; in 6.7% of children - with congenital and hereditary nephropathies; in 4.4% of children an outcome of a hemolytic uremic syndrome. The observed children dominated by I-II (74.3%), less often III and IV (25.7%) stages of CKD. The revealed clinical and paraclinical features of CKD in children are presented. The modern principles of early diagnosis of CKD in children and the identification of risk factors for the progression of nephropathy have been substantiated. For the diagnosis of CKD in childhood there has been created a. n algorithm, including at the outpatient stage. Authors suggested a set of measures for the prevention of nephropathy. Conclusion. For early diagnosis of CKD in childhood there was developed an algorithm based on the analysis of a complex of clinical and paraclinical, structural and functional parameters of the kidneys in combination with the parameters of endothelial function and cytokine status.

Ocular changes in some progressive hereditary nephropathies

1987 ◽  
Vol 1 (3) ◽  
pp. 525-530 ◽  
Author(s):  
J. L. Dufier ◽  
D. Orssaud ◽  
P. Dhermy ◽  
M. C. Gubler ◽  
M. F. Gagnadoux ◽  
...  
Keyword(s):  
Ocular Changes ◽  
Hereditary Nephropathies

Hereditary Nephropathies

2005 ◽  
pp. 140-140 ◽  
Author(s):  
RN Srivastava ◽  
Arvind Bagga
Keyword(s):  
Hereditary Nephropathies

Current Status of DNA Diagnosis for Hereditary Nephropathies

1996 ◽  
Vol 19 (3-4) ◽  
pp. 209-214 ◽  
Author(s):  
Klaus Zerres ◽  
Sabine Rudnik-Schöneborn
Keyword(s):  
Current Status ◽  
Dna Diagnosis ◽  
Hereditary Nephropathies
Sign in / Sign up

Export Citation Format

Share Document