Sudden infant death syndrome classification: Difference between revisions
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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. | 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 | OR |
Revision as of 14:10, 20 February 2020
Sudden infant death syndrome Microchapters |
Differentiating Sudden infant death syndrome from other Diseases |
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Sudden infant death syndrome classification On the Web |
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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
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
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][4][5][6][7]
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.
- ↑ Tan BH, Pundi KN, Van Norstrand DW, Valdivia CR, Tester DJ, Medeiros-Domingo A; et al. (2010). "Sudden infant death syndrome-associated mutations in the sodium channel beta subunits". Heart Rhythm. 7 (6): 771–8. doi:10.1016/j.hrthm.2010.01.032. PMC 2909680. PMID 20226894.
- ↑ Otagiri T, Kijima K, Osawa M, Ishii K, Makita N, Matoba R; et al. (2008). "Cardiac ion channel gene mutations in sudden infant death syndrome". Pediatr Res. 64 (5): 482–7. doi:10.1203/PDR.0b013e3181841eca. PMID 18596570.
- ↑ Tester DJ, Tan BH, Medeiros-Domingo A, Song C, Makielski JC, Ackerman MJ (2011). "Loss-of-function mutations in the KCNJ8-encoded Kir6.1 K(ATP) channel and sudden infant death syndrome". Circ Cardiovasc Genet. 4 (5): 510–5. doi:10.1161/CIRCGENETICS.111.960195. PMC 3281577. PMID 21836131.
- ↑ Tester DJ, Wong LCH, Chanana P, Jaye A, Evans JM, FitzPatrick DR; et al. (2018). "Cardiac Genetic Predisposition in Sudden Infant Death Syndrome". J Am Coll Cardiol. 71 (11): 1217–1227. doi:10.1016/j.jacc.2018.01.030. PMID 29544605.