Andersen-Tawil syndrome differential diagnosis: Difference between revisions
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{{Andersen-Tawil syndrome}} | {{Andersen-Tawil syndrome}} | ||
{{CMG}}; {{AE}} {{ | {{CMG}}; {{AE}} {{VKG}} | ||
== Overview == | == Overview == | ||
Andersen-Tawil syndrome must be differentiated from [[Romano-Ward syndrome]], [[Timothy syndrome]], [[Jervell and Lange-Nielsen syndrome]] (JLNS), [[Brugada syndrome]], [[Sudden infant death syndrome]] ([[Sudden infant death syndrome|SIDS]]), [[Hypokalemic periodic paralysis]], [[Hyperkalemic periodic paralysis]] and Thyrotoxic [[periodic paralysis]]. | |||
==Differentiating Andersen-Tawil syndrome from other Diseases== | ==Differentiating Andersen-Tawil syndrome from other Diseases== | ||
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{{WikiDoc Sources}} | {{WikiDoc Sources}} | ||
[[ | [[Category:Rare Disease]] | ||
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[[Category:Genetic disorders]] | [[Category:Genetic disorders]] | ||
Revision as of 14:51, 13 February 2020
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Vamsikrishna Gunnam M.B.B.S [2]
Overview
Andersen-Tawil syndrome must be differentiated from Romano-Ward syndrome, Timothy syndrome, Jervell and Lange-Nielsen syndrome (JLNS), Brugada syndrome, Sudden infant death syndrome (SIDS), Hypokalemic periodic paralysis, Hyperkalemic periodic paralysis and Thyrotoxic periodic paralysis.
Differentiating Andersen-Tawil syndrome from other Diseases
- Andersen-Tawil syndrome must be differentiated from the following diseases: