Clinical Evaluation of Nephrotic Syndrome Manifesting in the First Year of Life

2009 ◽  
Vol 13 (2) ◽  
pp. 161
Author(s):  
Sung Hee Cho ◽  
Joo Hoon Lee ◽  
Young Mi Cho ◽  
Young Seo Park ◽  
Hae Il Cheong
PEDIATRICS ◽  
1960 ◽  
Vol 25 (6) ◽  
pp. 967-976
Author(s):  
R. A. Parker ◽  
Carolyn F. Piel

The clinical course of nephrosis in five infants with onset of disease before 7 months of age is presented, together with evaluation of renal lesions seen at necropsy. The problems of the management of nephrosis susceptibility to infection and water and electrolyte imbalance were found to be exaggerated by the young age of the patients. The renal pathology observed in these five infants consisted of persistence of immature glomeruli and dilatation of the tubules in the cortical area. Later, the immature glomeruli and associated tubules appear to atrophy and the remaining glomeruli to hypertrophy. Long-term adrenocorticosteroid therapy seems to be contraindicated, not only on the basis of the pathologic changes, but because it greatly exaggerates the problems of management and does not effect a remission of the disease.


2010 ◽  
Vol 53 (3) ◽  
pp. 157-159 ◽  
Author(s):  
Sylva Skálová ◽  
Miroslav Podhola ◽  
Karel Vondrák ◽  
Gil Chernin

Podocin mutations (NPHS2 gene) are mostly responsible for steroid-resistant nephrotic syndrome (SRNS) of childhood onset. Patients with NPHS2 gene mutations do not respond to corticoids and other immunosuppressive agents; partial remission can be rarely induced by cyclosporin A. We present a boy, where SRNS was diagnosed within first year of life. By the age of 15 years, proteinuria reached 9000 mg/24 h, cholesterolemia 15 mmol/L, albuminemia 19.6 g/L, in spite of combined therapy with cyclosporine A, methylprednisolone, enalapril and losartan. At that time a combined heterozygous form of two NPHS2 gene mutations (p.R138Q and p.V290M) was diagnosed, methylprednisolone was discontinued and patient underwent ten plasmapheresis procedures. This resulted in clinical improvement (proteinuria 3000 mg/24 h, S-cholesterol 6 mmol/L, albumin 30g/L) lasting for three years. In conclusion, plasmapheresis can result in clinical improvement and stabilization of SRNS caused by podocine mutation, before renal replacement therapy is initiated.


2012 ◽  
Vol 2 (1) ◽  
pp. 22 ◽  
Author(s):  
Manisha Sahay ◽  
Swarnalatha Gowrishankar ◽  
Girish Narayen ◽  
Anuradha

2020 ◽  
Vol 24 (3) ◽  
pp. 167-173
Author(s):  
Ludmila A. Deryugina ◽  
T. V. Otpuschennikova

The aim of the study was to study the formation of urination in young children, taking into account perinatal factors. Material and methods. the pattern of urination was studied in 42 patients at the stages of antenatal observation, after birth during the first year of life and at the age of three. Clinical evaluation of urination was performed in young children using a developed qualimetric table that takes into account the volume of the bladder and frequency of urination, the nature of urination, the presence of urge to urinate and behavioral reactions. At the age of three, a qualimetric table was used to evaluate E. L. Vishnevsky’s urination (2001). The observation group consisted of 42 patients whose urination pattern was studied at the stages of antenatal observation, during the first year of life and at the age of three. The features of the course of the antenatal and postnatal period of children’s development were taken into account: pregnancy complications, fetal pathological conditions, features of the morpho-functional state of infants, and neurological comorbidities. Results. According to the results of clinical evaluation of urination in children at 3 years of age, 3 groups of children were identified: with “Mature”,”delayed formation of “Mature” type of urination”, as well as “dysfunctional type of urination”. Conclusions. the manifestations of “maturity of urination” in infants at the age of 1 year are the compliance of hydrodynamic indicators with age standards, the formation of continuous urination, signs of controlling behavior: behavioral reaction to the urge, the absence of” missing urine “during the day, during daytime and nighttime sleep, “urination on request”. The “delay in the formation of mature urination type”, the formation of “dysfunctional urination type “ revealed the determining influence of the pathological course of the antenatal period of child development, the implementation of signs of pathological fetal urination, the presence of neurological symptoms and signs of morpho-functional immaturity of the postnatal period. “Dysfunctional urination” was manifested by: a decrease in the capacity of the bladder and the discrepancy between the hydrodynamic characteristics of the age parameters; monotony of the volume characteristics of the bladder during the day; imperative contractions of the bladder, that is, the presence of “wet gaps” between urination; urination during sleep; as well as a delay or lack of urge to urinate, behavioral responses and neatness skills.


1989 ◽  
Vol 9 (3) ◽  
pp. 140-146 ◽  
Author(s):  
M.B. Abdurrahman ◽  
F.H. Shipkey ◽  
A.T.H. Elidrissy ◽  
W. Al-Kahtani

1977 ◽  
Vol 90 (3) ◽  
pp. 415-417 ◽  
Author(s):  
E.C. Kohaut ◽  
L. Leighton Hill

2015 ◽  
Vol 47 (1) ◽  
pp. 38-41 ◽  
Author(s):  
S. Martínez Mejía ◽  
A. Alonso Melgar ◽  
M. Melgosa Hijosa ◽  
C. Fernandez Camblor ◽  
A. Peña Carrión ◽  
...  

1997 ◽  
Vol 41 (1) ◽  
pp. 156-156
Author(s):  
A Bojórquez-Ochoa ◽  
Bojorges B De León ◽  
Puente S García de la ◽  
S Zaltzman

Sign in / Sign up

Export Citation Format

Share Document