Alagille syndrome associated conditions: Difference between revisions
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==Associated Conditions== | ==Associated Conditions== | ||
Alagille syndrome can be associated with [[congenital heart disease]], particularly [[Tetralogy of Fallot]]. The[[kidney]]s and [[central nervous system]] may also be affected. Cases of unilateral coronal craniosynostosis have also been described in association with this syndrome. | Alagille syndrome can be associated with [[congenital heart disease]], particularly [[Tetralogy of Fallot]]. The [[kidney]]s and [[central nervous system]] may also be affected. Cases of unilateral coronal craniosynostosis have also been described in association with this syndrome. | ||
==References== | ==References== | ||
{{reflist|2}} | {{reflist|2}} | ||
{{WH}} | |||
{{WS}} | |||
[[Category:Pediatrics]] | [[Category:Pediatrics]] | ||
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[[Category:Rare diseases]] | [[Category:Rare diseases]] | ||
[[Category:Hepatology]] | [[Category:Hepatology]] | ||
[[Category: | [[Category:Overview complete]] | ||
Latest revision as of 18:30, 17 April 2012
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Alagille syndrome Microchapters |
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Alagille syndrome associated conditions On the Web |
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Overview
Alagille syndrome is a multisystem genetic disorder that affects the liver, heart, eyes,face, skeleton, kidneys and vascular system.
Associated Conditions
Alagille syndrome can be associated with congenital heart disease, particularly Tetralogy of Fallot. The kidneys and central nervous system may also be affected. Cases of unilateral coronal craniosynostosis have also been described in association with this syndrome.