Andersen-Tawil syndrome differential diagnosis: Difference between revisions
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{{Andersen-Tawil syndrome}} | {{Andersen-Tawil syndrome}} | ||
{{CMG}}; {{AE}} {{ | {{CMG}}; {{AE}} {{VKG}} | ||
== 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== | ||
Andersen-Tawil syndrome | |||
* 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><ref name="pmid17210839">{{cite journal| author=Arnestad M, Crotti L, Rognum TO, Insolia R, Pedrazzini M, Ferrandi C et al.| title=Prevalence of long-QT syndrome gene variants in sudden infant death syndrome. | journal=Circulation | year= 2007 | volume= 115 | issue= 3 | pages= 361-7 | pmid=17210839 | doi=10.1161/CIRCULATIONAHA.106.658021 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=17210839 }}</ref><ref name="pmid11136691">{{cite journal| author=Schwartz PJ, Priori SG, Spazzolini C, Moss AJ, Vincent GM, Napolitano C et al.| title=Genotype-phenotype correlation in the long-QT syndrome: gene-specific triggers for life-threatening arrhythmias. | journal=Circulation | year= 2001 | volume= 103 | issue= 1 | pages= 89-95 | pmid=11136691 | doi=10.1161/01.cir.103.1.89 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=11136691 }}</ref><ref name="pmid16012827">{{cite journal| author=Wedekind H, Bajanowski T, Friederich P, Breithardt G, Wülfing T, Siebrands C et al.| title=Sudden infant death syndrome and long QT syndrome: an epidemiological and genetic study. | journal=Int J Legal Med | year= 2006 | volume= 120 | issue= 3 | pages= 129-37 | pmid=16012827 | doi=10.1007/s00414-005-0019-0 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=16012827 }}</ref><ref name="pmid27761167">{{cite journal| author=Juang JJ, Horie M| title=Genetics of Brugada syndrome. | journal=J Arrhythm | year= 2016 | volume= 32 | issue= 5 | pages= 418-425 | pmid=27761167 | doi=10.1016/j.joa.2016.07.012 | pmc=5063259 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=27761167 }}</ref><ref name="pmid15950200">{{cite journal| author=Thomas D, Wimmer AB, Karle CA, Licka M, Alter M, Khalil M et al.| title=Dominant-negative I(Ks) suppression by KCNQ1-deltaF339 potassium channels linked to Romano-Ward syndrome. | journal=Cardiovasc Res | year= 2005 | volume= 67 | issue= 3 | pages= 487-97 | pmid=15950200 | doi=10.1016/j.cardiores.2005.05.003 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=15950200 }}</ref> | |||
* Hypokalemic periodic paralysis | **[[Romano-Ward syndrome]] | ||
* Hyperkalemic periodic paralysis | ** [[Timothy syndrome]] | ||
* Thyrotoxic periodic paralysis | ** [[Jervell and Lange-Nielsen syndrome]] (JLNS) | ||
** [[Brugada syndrome]] | |||
** [[Sudden infant death syndrome]] ([[Sudden infant death syndrome|SIDS]]) | |||
** [[Hypokalemic periodic paralysis]] | |||
** [[Hyperkalemic periodic paralysis]] | |||
** Thyrotoxic [[periodic paralysis]] | |||
==References== | ==References== | ||
{{Reflist|2}} | {{Reflist|2}} | ||
{{WikiDoc Help Menu}} | {{WikiDoc Help Menu}} | ||
{{WikiDoc Sources}} | {{WikiDoc Sources}} | ||
[[Category:Rare Disease]] | |||
[[Category:Cardiology]] | |||
[[Category:Genetic disorders]] | |||
Latest revision as of 14:55, 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.
- ↑ Arnestad M, Crotti L, Rognum TO, Insolia R, Pedrazzini M, Ferrandi C; et al. (2007). "Prevalence of long-QT syndrome gene variants in sudden infant death syndrome". Circulation. 115 (3): 361–7. doi:10.1161/CIRCULATIONAHA.106.658021. PMID 17210839.
- ↑ Schwartz PJ, Priori SG, Spazzolini C, Moss AJ, Vincent GM, Napolitano C; et al. (2001). "Genotype-phenotype correlation in the long-QT syndrome: gene-specific triggers for life-threatening arrhythmias". Circulation. 103 (1): 89–95. doi:10.1161/01.cir.103.1.89. PMID 11136691.
- ↑ Wedekind H, Bajanowski T, Friederich P, Breithardt G, Wülfing T, Siebrands C; et al. (2006). "Sudden infant death syndrome and long QT syndrome: an epidemiological and genetic study". Int J Legal Med. 120 (3): 129–37. doi:10.1007/s00414-005-0019-0. PMID 16012827.
- ↑ Juang JJ, Horie M (2016). "Genetics of Brugada syndrome". J Arrhythm. 32 (5): 418–425. doi:10.1016/j.joa.2016.07.012. PMC 5063259. PMID 27761167.
- ↑ Thomas D, Wimmer AB, Karle CA, Licka M, Alter M, Khalil M; et al. (2005). "Dominant-negative I(Ks) suppression by KCNQ1-deltaF339 potassium channels linked to Romano-Ward syndrome". Cardiovasc Res. 67 (3): 487–97. doi:10.1016/j.cardiores.2005.05.003. PMID 15950200.