Andersen-Tawil syndrome differential diagnosis: Difference between revisions
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==Differentiating Andersen-Tawil syndrome from other Diseases== | ==Differentiating Andersen-Tawil syndrome from other Diseases== | ||
* Andersen-Tawil syndrome must be differentiated from the following diseases:<ref name="pmid20301308">{{cite journal| author=Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Stephens K et al.| title=GeneReviews® | journal= | year= 1993 | volume= | issue= | pages= | pmid=20301308 | doi= | pmc= | url= }}</ref> | * Andersen-Tawil syndrome must be differentiated from the following diseases:<ref name="pmid20301308">{{cite journal| author=Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Stephens K et al.| title=GeneReviews® | journal= | year= 1993 | volume= | issue= | pages= | pmid=20301308 | doi= | pmc= | url= }}</ref><ref name="pmid11710892">{{cite journal| author=Ackerman MJ, Siu BL, Sturner WQ, Tester DJ, Valdivia CR, Makielski JC et al.| title=Postmortem molecular analysis of SCN5A defects in sudden infant death syndrome. | journal=JAMA | year= 2001 | volume= 286 | issue= 18 | pages= 2264-9 | pmid=11710892 | doi=10.1001/jama.286.18.2264 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=11710892 }}</ref> | ||
**[[Romano-Ward syndrome]] | **[[Romano-Ward syndrome]] | ||
** [[Timothy syndrome]] | ** [[Timothy syndrome]] | ||
Revision as of 14:53, 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
References
- ↑ Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Stephens K; et al. (1993). "GeneReviews®". PMID 20301308.
- ↑ Ackerman MJ, Siu BL, Sturner WQ, Tester DJ, Valdivia CR, Makielski JC; et al. (2001). "Postmortem molecular analysis of SCN5A defects in sudden infant death syndrome". JAMA. 286 (18): 2264–9. doi:10.1001/jama.286.18.2264. PMID 11710892.