Sudden infant death syndrome classification: Difference between revisions
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==Classification== | ==Classification== | ||
There is no established system for the classification of Sudden infant death syndrome.<ref name="pmid17210841">{{cite journal| author=Wang DW, Desai RR, Crotti L, Arnestad M, Insolia R, Pedrazzini M | display-authors=etal| title=Cardiac sodium channel dysfunction in sudden infant death syndrome. | journal=Circulation | year= 2007 | volume= 115 | issue= 3 | pages= 368-76 | pmid=17210841 | doi=10.1161/CIRCULATIONAHA.106.646513 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=17210841 }}</ref><ref name="pmid17210839">{{cite journal| author=Arnestad M, Crotti L, Rognum TO, Insolia R, Pedrazzini M, Ferrandi C | display-authors=etal| 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> | There is no established system for the classification of Sudden infant death syndrome.<ref name="pmid17210841">{{cite journal| author=Wang DW, Desai RR, Crotti L, Arnestad M, Insolia R, Pedrazzini M | display-authors=etal| title=Cardiac sodium channel dysfunction in sudden infant death syndrome. | journal=Circulation | year= 2007 | volume= 115 | issue= 3 | pages= 368-76 | pmid=17210841 | doi=10.1161/CIRCULATIONAHA.106.646513 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=17210841 }}</ref><ref name="pmid17210839">{{cite journal| author=Arnestad M, Crotti L, Rognum TO, Insolia R, Pedrazzini M, Ferrandi C | display-authors=etal| 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="pmid17967976">{{cite journal| author=Van Norstrand DW, Valdivia CR, Tester DJ, Ueda K, London B, Makielski JC | display-authors=etal| title=Molecular and functional characterization of novel glycerol-3-phosphate dehydrogenase 1 like gene (GPD1-L) mutations in sudden infant death syndrome. | journal=Circulation | year= 2007 | volume= 116 | issue= 20 | pages= 2253-9 | pmid=17967976 | doi=10.1161/CIRCULATIONAHA.107.704627 | pmc=3332545 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=17967976 }}</ref> | ||
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Revision as of 12:46, 19 February 2020
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Sudden infant death syndrome Microchapters |
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Differentiating Sudden infant death syndrome from other Diseases |
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Diagnosis |
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Treatment |
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Case Studies |
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Sudden infant death syndrome classification On the Web |
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American Roentgen Ray Society Images of Sudden infant death syndrome classification |
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Risk calculators and risk factors for Sudden infant death syndrome classification |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Vamsikrishna Gunnam M.B.B.S [2]
Overview
There is no established system for the classification of Sudden infant death syndrome. Sudden infant death syndrome (SIDS) is a rare syndrome which follows autosomal recessive pattern of inheritance and have mutations in SCN5A gene and other genes but is not clear.
OR
[Disease name] may be classified according to [classification method] into [number] subtypes/groups: [group1], [group2], [group3], and [group4].
OR
[Disease name] may be classified into [large number > 6] subtypes based on [classification method 1], [classification method 2], and [classification method 3]. [Disease name] may be classified into several subtypes based on [classification method 1], [classification method 2], and [classification method 3].
OR
Based on the duration of symptoms, [disease name] may be classified as either acute or chronic.
OR
If the staging system involves specific and characteristic findings and features: According to the [staging system + reference], there are [number] stages of [malignancy name] based on the [finding1], [finding2], and [finding3]. Each stage is assigned a [letter/number1] and a [letter/number2] that designate the [feature1] and [feature2].
OR
The staging of [malignancy name] is based on the [staging system].
OR
There is no established system for the staging of [malignancy name].
Classification
There is no established system for the classification of Sudden infant death syndrome.[1][2][3]
| Phenotype | Gene involved | Location | Inheritance pattern |
| Sudden infant death syndrome | SCN5A
SCN4A KCNQ1 KCNH2 RYR2 |
3p22.2 | Autosomal recessive |
OR
[Disease name] may be classified according to [classification method] into [number] subtypes/groups:
- [Group1]
- [Group2]
- [Group3]
- [Group4]
OR
[Disease name] may be classified into [large number > 6] subtypes based on:
- [Classification method 1]
- [Classification method 2]
- [Classification method 3]
[Disease name] may be classified into several subtypes based on:
- [Classification method 1]
- [Classification method 2]
- [Classification method 3]
OR
Based on the duration of symptoms, [disease name] may be classified as either acute or chronic.
OR
If the staging system involves specific and characteristic findings and features:
According to the [staging system + reference], there are [number] stages of [malignancy name] based on the [finding1], [finding2], and [finding3]. Each stage is assigned a [letter/number1] and a [letter/number2] that designate the [feature1] and [feature2].
OR
The staging of [malignancy name] is based on the [staging system].
OR
There is no established system for the staging of [malignancy name].
References
- ↑ Wang DW, Desai RR, Crotti L, Arnestad M, Insolia R, Pedrazzini M; et al. (2007). "Cardiac sodium channel dysfunction in sudden infant death syndrome". Circulation. 115 (3): 368–76. doi:10.1161/CIRCULATIONAHA.106.646513. PMID 17210841.
- ↑ 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.
- ↑ Van Norstrand DW, Valdivia CR, Tester DJ, Ueda K, London B, Makielski JC; et al. (2007). "Molecular and functional characterization of novel glycerol-3-phosphate dehydrogenase 1 like gene (GPD1-L) mutations in sudden infant death syndrome". Circulation. 116 (20): 2253–9. doi:10.1161/CIRCULATIONAHA.107.704627. PMC 3332545. PMID 17967976.