Analbuminaemia: Difference between revisions
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==Overview== | |||
'''Analbuminaemia''' is a genetically inherited [[metabolism|metabolic defect]] characterised by an impaired synthesis of [[human serum albumin|serum albumin]].<ref>{{cite journal |author=Watkins S, Madison J, Galliano M, Minchiotti L, Putnam FW |title=Analbuminemia: three cases resulting from different point mutations in the albumin gene |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=91 |issue=20 |pages=9417-21 |year=1994 |pmid=7937781 |doi=}}</ref> Despite the fact that albumin is the most common serum protein, analbuminemia is a benign condition. | '''Analbuminaemia''' is a genetically inherited [[metabolism|metabolic defect]] characterised by an impaired synthesis of [[human serum albumin|serum albumin]].<ref>{{cite journal |author=Watkins S, Madison J, Galliano M, Minchiotti L, Putnam FW |title=Analbuminemia: three cases resulting from different point mutations in the albumin gene |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=91 |issue=20 |pages=9417-21 |year=1994 |pmid=7937781 |doi=}}</ref> Despite the fact that albumin is the most common serum protein, analbuminemia is a benign condition. | ||
==References== | ==References== | ||
{{Reflist|2}} | |||
[[pl:Analbuminemia]] | [[pl:Analbuminemia]] | ||
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[[Category:Inborn errors of metabolism]] | [[Category:Inborn errors of metabolism]] | ||
[[Category:Hematology]] | [[Category:Hematology]] | ||
[[Category:Gastroenterology]] |
Revision as of 14:16, 2 September 2012
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Overview
Analbuminaemia is a genetically inherited metabolic defect characterised by an impaired synthesis of serum albumin.[1] Despite the fact that albumin is the most common serum protein, analbuminemia is a benign condition.