Fanconi-Albertini-Zellweger syndrome: Difference between revisions

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{{CMG}}; '''Associate Editor(s)-In-Chief:''' {{CZ}}, [[User:Raviteja Reddy Guddeti|Raviteja Guddeti, M.B.B.S.]][mailto:rgudetti@perfuse.org]
{{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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==Overview==
A rare syndrome characterized mainly by [[congenital heart defect]], brain abnormalities, [[osteoporosis]], blood abnormalities, unusual face and [[metabolic acidosis]].
 


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==
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{{Reflist|2}}


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[[Category:Pediatrics]]
[[Category:Pediatrics]]
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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]

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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.

References

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