Sudden infant death syndrome pathophysiology: Difference between revisions
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'''Genetics''' | '''Genetics''' | ||
* The exact involvement of genetic changes is not clear in the pathogenesis of Sudden infant death syndrome (SIDS) | * The exact involvement of genetic changes is not clear in the pathogenesis of Sudden infant death syndrome (SIDS)<ref name="pmid10401808">{{cite journal| author=Malloy MH, Freeman DH| title=Sudden infant death syndrome among twins. | journal=Arch Pediatr Adolesc Med | year= 1999 | volume= 153 | issue= 7 | pages= 736-40 | pmid=10401808 | doi=10.1001/archpedi.153.7.736 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=10401808 }}</ref> | ||
* With the recent research we can say that Sudden infant death syndrome (SIDS) is not a genetic disorder but identification of genetic polymorphisms along with the risk factors increase the risk of developing susceptibility to Sudden infant death syndrome (SIDS). | * With the recent research we can say that Sudden infant death syndrome (SIDS) is not a genetic disorder but identification of genetic polymorphisms along with the risk factors increase the risk of developing susceptibility to Sudden infant death syndrome (SIDS). | ||
Revision as of 23:41, 19 February 2020
Sudden infant death syndrome Microchapters |
Differentiating Sudden infant death syndrome from other Diseases |
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Diagnosis |
Treatment |
Case Studies |
Sudden infant death syndrome pathophysiology On the Web |
American Roentgen Ray Society Images of Sudden infant death syndrome pathophysiology |
Risk calculators and risk factors for Sudden infant death syndrome pathophysiology |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Vamsikrishna Gunnam M.B.B.S [2]
Overview
The exact pathogenesis of Sudden infant death syndrome (SIDS) is not fully understood. It is thought that Sudden infant death syndrome (SIDS) may be caused by either genetic mutations, brainstem abnormality, airflow obstruction, maternal smoking, or infection.
OR
[Pathogen name] is usually transmitted via the [transmission route] route to the human host.
OR
Following transmission/ingestion, the [pathogen] uses the [entry site] to invade the [cell name] cell.
OR
[Disease or malignancy name] arises from [cell name]s, which are [cell type] cells that are normally involved in [function of cells].
OR
The progression to [disease name] usually involves the [molecular pathway].
OR
The pathophysiology of [disease/malignancy] depends on the histological subtype.
Pathophysiology
Physiology
The normal physiology of [name of process] can be understood as follows:
Pathogenesis
- The exact pathogenesis of Sudden infant death syndrome (SIDS) is not completely understood.
- The pathogenesis of Sudden infant death syndrome (SIDS) involves the following:
Genetics
- The exact involvement of genetic changes is not clear in the pathogenesis of Sudden infant death syndrome (SIDS)[1]
- With the recent research we can say that Sudden infant death syndrome (SIDS) is not a genetic disorder but identification of genetic polymorphisms along with the risk factors increase the risk of developing susceptibility to Sudden infant death syndrome (SIDS).
OR
- It is understood that [disease name] is the result of / is mediated by / is produced by / is caused by either [hypothesis 1], [hypothesis 2], or [hypothesis 3].
- [Pathogen name] is usually transmitted via the [transmission route] route to the human host.
- Following transmission/ingestion, the [pathogen] uses the [entry site] to invade the [cell name] cell.
- [Disease or malignancy name] arises from [cell name]s, which are [cell type] cells that are normally involved in [function of cells].
- The progression to [disease name] usually involves the [molecular pathway].
- The pathophysiology of [disease/malignancy] depends on the histological subtype.
Genetics
[Disease name] is transmitted in [mode of genetic transmission] pattern.
OR
Genes involved in the pathogenesis of [disease name] include:
- [Gene1]
- [Gene2]
- [Gene3]
OR
The development of [disease name] is the result of multiple genetic mutations such as:
- [Mutation 1]
- [Mutation 2]
- [Mutation 3]
Associated Conditions
Conditions associated with [disease name] include:
- [Condition 1]
- [Condition 2]
- [Condition 3]
Gross Pathology
On gross pathology, [feature1], [feature2], and [feature3] are characteristic findings of [disease name].
Microscopic Pathology
On microscopic histopathological analysis, [feature1], [feature2], and [feature3] are characteristic findings of [disease name].
References
- ↑ Malloy MH, Freeman DH (1999). "Sudden infant death syndrome among twins". Arch Pediatr Adolesc Med. 153 (7): 736–40. doi:10.1001/archpedi.153.7.736. PMID 10401808.