Fanconi-Albertini-Zellweger syndrome: Difference between revisions
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Created page with "__NOTOC__ {{CMG}}; '''Associate Editor(s)-In-Chief:''' {{CZ}}, Raviteja Guddeti, M.B.B.S.[mailto:rgudetti@perfuse.org] ==Overview== A rare s..." |
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==Overview== | ==Overview== | ||
A rare syndrome characterized mainly by [[congenital heart defect]], brain abnormalities, [[osteoporosis]], blood abnormalities, unusual face and [[metabolic acidosis]]. | A rare syndrome characterized mainly by [[congenital heart defect]], brain abnormalities, [[osteoporosis]], blood abnormalities, unusual face and [[metabolic acidosis]]. | ||
Revision as of 03:28, 23 July 2012
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-In-Chief: Cafer Zorkun, M.D., Ph.D. [2], Raviteja Guddeti, M.B.B.S.[3]
Overview
A rare syndrome characterized mainly by congenital heart defect, brain abnormalities, osteoporosis, blood abnormalities, unusual face and metabolic acidosis.
References