Cardiac tumors causes: Difference between revisions
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==Causes== | ==Causes== | ||
*Many genetic conditions are strongly associated with a large number of heart tumors. Some of them are as follows: | *Many genetic conditions are strongly associated with a large number of heart tumors. Some of them are as follows:<ref name="pmid29214333">{{cite journal| author=Lee E, Mahani MG, Lu JC, Dorfman AL, Srinivasan A, Agarwal PP| title=Primary cardiac tumors associated with genetic syndromes: a comprehensive review. | journal=Pediatr Radiol | year= 2018 | volume= 48 | issue= 2 | pages= 156-164 | pmid=29214333 | doi=10.1007/s00247-017-4027-2 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=29214333 }} </ref> | ||
{| class="wikitable" | {| class="wikitable" | ||
|+ Cardiac tumors genetic causes | |+ Cardiac tumors genetic causes | ||
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| [[Paraganglioma]] || [[Neurofibromatosis type 1]] || NF1 gene | | [[Paraganglioma]] || [[Neurofibromatosis type 1]] || NF1 gene | ||
|} | |} | ||
==References== | ==References== | ||
Revision as of 20:54, 23 May 2022
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Overview
Causes
- Many genetic conditions are strongly associated with a large number of heart tumors. Some of them are as follows:[1]
| Tumor | Syndrome | Gene Associated with syndrome |
|---|---|---|
| Rhabdomyoma | Tuberous Sclerosis | TSC1 or hamartin
TSC2 or tuberin |
| Fibroma | Gorlin Syndrome | PATCHED gene |
| Myxoma | Carney Complex | Inactivating mutation of PRKARA1A
Activating pathogenic variant of PRKACA gene |
| Paraganglioma | Carney triad | No known gene associations |
| Paraganglioma | Hereditary Paraganglioma | Mutation of succinate dehydrogenase subunit
SDHAF2 gene, and possibly MAX gene but these mutations are rare |
| Paraganglioma | Von Hippel Lindau | VHL gene |
| Paraganglioma | Neurofibromatosis type 1 | NF1 gene |
References
- ↑ Lee E, Mahani MG, Lu JC, Dorfman AL, Srinivasan A, Agarwal PP (2018). "Primary cardiac tumors associated with genetic syndromes: a comprehensive review". Pediatr Radiol. 48 (2): 156–164. doi:10.1007/s00247-017-4027-2. PMID 29214333.