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Severe hypoalphalipoproteinaemia in a child with acute post-streptococcal glomerulonephritis (APSGN)
Mohammad B Alayli1, Sami A Sanjad
1Department of Pediatrics, American University of Beirut, Beirut, Lebanon.
Abstract:
We describe a child with acute post-streptococcal glomerulonephritis (APSGN), who developed a very low plasma high-density lipoprotein cholesterol (α-lipoprotein) in association with transient but massive proteinuria. The hypoalphalipoproteinaemia resolved spontaneously concomitant with the remission in proteinuria and the patient had a complete clinical recovery. Urinary loss of apolipoprotein A1 may have contributed to the hypoalphalipoproteinaemia. To our knowledge, this has not been reported previously in APSGN.
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