Familial hemolytic-uremic syndrome and homozygous factor H deficiency

Inherited hemolytic-uremic syndrome (HUS) is unusual. We report the occurrence of HUS in two siblings; one died at an early age while the other (the proband) has presented with three episodes of HUS since the age of 19 years. The finding of a persistently low serum C3 level in this patient led to a...

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Veröffentlicht in:	American journal of kidney diseases 1994-12, Vol.24 (6), p.936-941
Hauptverfasser:	PICHETTE, V, QUERIN, S, SCHÜRCH, W, BRUN, G, LEHNER-NETSCH, G, DELAGE, J.-M
Format:	Artikel
Sprache:	eng
Schlagworte:	Adult Biological and medical sciences Complement Factor H - deficiency Complement System Proteins - analysis Female Hemolytic-Uremic Syndrome - genetics Hemolytic-Uremic Syndrome - therapy Homozygote Humans Kidneys Medical sciences Nephrology. Urinary tract diseases Pedigree Urinary system involvement in other diseases. Miscellaneous
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