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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{{CMG}}; '''Associate Editor(s)-In-Chief:''' {{CZ}}, [[User:Raviteja Reddy Guddeti|Raviteja Guddeti, M.B.B.S.]][mailto: | {{CMG}}; '''Associate Editor(s)-In-Chief:''' {{CZ}}, [[User:Raviteja Reddy Guddeti|Raviteja Guddeti, M.B.B.S.]][mailto:ravitheja.g@gmail.com] | ||
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Fanconi-Albertini-Zellweger syndrome is a rare syndrome that is typically characterized by [[congenital heart defect]]s, brain abnormalities, [[osteoporosis]], blood abnormalities, unusual facial characteristics, and [[metabolic acidosis]]. | |||
==References== | ==References== | ||
{{Reflist|2}} | {{Reflist|2}} | ||
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{{WS}} | |||
[[Category:Pediatrics]] | [[Category:Pediatrics]] | ||
Latest revision as of 20:39, 1 August 2013
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]
Fanconi-Albertini-Zellweger syndrome is a rare syndrome that is typically characterized by congenital heart defects, brain abnormalities, osteoporosis, blood abnormalities, unusual facial characteristics, and metabolic acidosis.