نتایج جستجو برای: resistant nephrotic syndrome
تعداد نتایج: 804441 فیلتر نتایج به سال:
The aim of our study was to examine NPHS1, NPHS2, WT1 and LAMB2 mutations, previously reported in two thirds of patients with nephrotic syndrome with onset before the age of one year old. Genomic DNA samples from Polish children (n=33) with Steroid-Resistant Nephrotic Syndrome (SRNS) due to focal segmental glomerulosclerosis (FSGS), manifesting before the age of 13 years old, underwent retrospe...
Steroid-resistant nephrotic syndrome (SRNS) is a frequent cause of progressive renal function decline and affects millions of people. In a recent study, 30% of SRNS cases evaluated were the result of monogenic mutations in 1 of 27 different genes. Here, using homozygosity mapping and whole-exome sequencing, we identified recessive mutations in kidney ankyrin repeat-containing protein 1 (KANK1),...
Chaib H, Hoskins BE, Ashraf S, Goyal M, Wiggins RC, Hildebrandt F. Identification of BRAF as a new interactor of PLCε1, the protein mutated in nephrotic syndrome type 3. Am J Physiol Renal Physiol 294: F93–F99, 2008. First published October 17, 2007; doi:10.1152/ajprenal.00345.2007.—Steroid-resistant nephrotic syndrome is a malfunction of the kidney glomerular filter that leads to proteinuria, ...
Nephrotic syndrome is a rare manifestation of renal artery stenosis, presented mainly in adulthood. This is the report of a 4 months old boy admitted for hypertension and nephrotic syndrome. Left renal artery stenosis and renal hypoplasia were documented by laboratory and imaging studies. Proteinuria improved with medical treatment, with no need to surgical repair. Blood pressure remained norma...
OBJECTIVE: To find out the pattern of glomerulopathies in paediatric population, undergoing renal biopsy at Khyber Teaching Hospital, Peshawar. METHODS: This was a prospective study carried out at the department of Nephrology at Khyber Teaching Hospital, Peshawar from June 2010 till June 2012. Ultrasound guided percutaneous renal biopsies were carried out in patients with the finding of; 1) Nep...
in this case report, we present the first diagnosed case of galloway- mowat syndrome in iran. a 7 month old infant boy with microcephaly that had prominently stunted head growth after birth, gastroesophageal reflux, multiple craniofascial characters, hypothyroidism and nephrotic syndrome diagnosed at 5 months of age associated with rapid decline in renal function and heavy proteinuria in 2 mont...
BACKGROUND Glomerulonephritis (GN) is a relatively rare disease with numerous subtypes. Most regional nephrology centres see only a limited number of patients with each type of GN every year. The objective of this study was to find out the pattern of glomerulopathies in paediatric population, undergoing renal biopsy in Peshawar. METHODS This was a prospective study carried out at the Departme...
Background. Nephrotic syndrome is caused by a variety of glomerulopathy. The current study investigated the renal histopathological spectrum of patients with nephrotic syndrome who received a renal biopsy in our department within the last 15 years. Methods. One thousand five hundred and twenty-three consecutive patients ( 14 years old at renal biopsy) with nephrotic syndrome were recruited. Pat...
BACKGROUND AND PURPOSE Thrombosis is one of the main complications of nephrotic syndrome; however, cerebral infarction associated with nephrotic syndrome has been rarely reported. SUMMARY OF REPORT We describe acute cerebral infarction in two young men with nephrotic syndrome. Both had a hypercoagulable state based on hemostatic studies. By retrospectively reviewing the medical records of the...
a 3-year-old girl was presented with periorbital edema, hypertension, proteinuria, and hematuria. she recovered clinically after 9 days with normal urinalysis. during the follow-up, she developed recurrent episodes of nephrotic syndrome. the kidney biopsy revealed mild mesangial proliferation and a low dose of prednisolone could effectively control the disease. iran j med sci 2005; 30(1): 38-40...
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