Childhood nephrosis followed by acute glomerulonephritis in adulthood.

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چکیده

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منابع مشابه

P96: Childhood Condition and Risky Behavior in Adulthood

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Childhood Nephrotic Syndrome (Nephrosis) — Treatment and Complications

Nephrotic syndrome is a common renal disorder in children, characterized by nephrotic range proteinuria, hypoalbuminemia, hyperlipidemia, and edema. The most common type is primary (idiopathic) associated with minimal change disease, which responds very well to steroid therapy and has a good long-term prognosis. Other causes, clinical presentation, laboratory findings, and management are discus...

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Childhood Nephrotic Syndrome (Nephrosis) — Treatment and Complications

Pediatric Nephrotic Syndrome is a renal disorder of children, characterized by nephrotic range proteinuria, hypoalbuminemia, hyperlipidemia and edema. The most common type is primary (idiopathic) associated with minimal change disease, which responds very well to steroid therapy and has a good long-term prognosis. Other causes, clinical presentation, laboratory findings and management are discu...

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Acute glomerulonephritis in children.

Acute glomerulonephritis (AGN) remains fairly common in the developing world although its frequency has declined in the industrial countries. The pattern of AGN was studied in one hundred hospitalised children. We recorded an increased prevalence in school age, i.e., 6-15 years (75%) and the occurrence of a streptococcal infection (90%), most often a pharyngeal infection (86%), one to three wee...

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Acute glomerulonephritis in infancy.

Karsner (1908) described 'congenital nephritis' in an infant who died 45 minutes after a normal birth, and Lapage (1932) discussed acute haemorrhagic nephritis in an 11-day-old boy who died in a few days. Conrad (1938) gave a resume of three infants with neonatal nephritis for which no cause was found. One infant died on the seventh day of life, but the others recovered. Generalized oedema, hae...

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ژورنال

عنوان ژورنال: BMJ

سال: 1967

ISSN: 0959-8138,1468-5833

DOI: 10.1136/bmj.1.5538.477