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Congenital nephrotic syndrome
- Congenital nephrotic syndrome is a kidney condition that begins in infancy and typically leads to irreversible kidney failure (end-stage renal disease) by early ...
- Congenital nephrotic syndrome is a disorder that is passed down through families in which a baby develops protein in ... Congenital nephrotic syndrome is an autosomal recessive genetic disorder. This means that each parent must pass on a copy ...
- Childhood nephrotic syndrome, nephrotic syndrome in children, congenital ... glomerulosclerosis, membranous nephropathy, minimal change disease, ...
- ... the NPHS1 gene have been found to cause congenital nephrotic syndrome. This condition is a kidney disorder that begins ... NPHS1 gene mutations account for all cases of congenital nephrotic syndrome of the Finnish type. This form of the ...
- ... the NPHS2 gene have been found to cause congenital nephrotic syndrome. This condition is a kidney disorder that begins ... appear to be the most frequent cause of congenital nephrotic syndrome. Most NPHS2 gene mutations change single protein building ...
- Kidney Diseases (National Library of Medicine)You have two kidneys, each about the size of your fist. They are near the middle of your back, just below the rib cage. Inside each kidney there are about ...
- ... This Health Condition MedlinePlus Genetics provides information about Congenital nephrotic syndrome More About This Health Condition MedlinePlus Genetics provides ...
- Ask the Experts: Pneumococcal (Immunization Action Coalition)Pneumococcal Infections/Prevention and Risk Factors ... Pneumococcal Infections ... Immunization Action Coalition ... Read answers by medical experts to healthcare provider ...
- Chronic Kidney Disease: Caring for Your Child (Nemours Foundation)... urethral valve obstruction, fetal hydronephrosis, vesicoureteral reflux, vur, ... bedwetting, enuresis, wetting the bed, nephrologist, nephrology, ...
- ... correction of fibrogen] alpha-chain gene (FGA) causes congenital afibrogenemia. J ... Linke RP. Nephrotic syndrome due to an amyloidogenic mutation in fibrinogen A ...