Metachondromatosis
Metachondromatosis is an autosomal dominant, [2] incompletely penetrant[3] skeletal disorder affecting the growth of bones, leading to multiple enchondromas and osteochondromas.[3] This tumor syndrome affects mainly tubular bones, though it can also involve the vertebrae, small joints, and flat bones.[4]
Metachondromatosis | |
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Other names | METCDS[1] |
Metachondromatosis has an autosomal dominant pattern of inheritance. |
Genetics
Metachondromatosis is inherited in an autosomal dominant manner.[3] This means that the defective gene responsible for a disorder is located on an autosome, and only one copy of the gene is sufficient to cause the disorder, when inherited from a parent who has the disorder.
Diagnosis
Treatment
gollark: It should be defined like this:```app.get("/path/:thing/bees", someHandlerFunction)```in your code somewhere.
gollark: No, your config file is literally just weird code.
gollark: Anything else is <:bees:724389994663247974> because it means your "config" is very strongly tied to the actual code.
gollark: > my current website serves various domains and uses different route configs for different domainsIf they're *very* different between each domain, then you should probably just specify the domains in the config file and have the routes per domain be fixed.
gollark: Specifically the bit before the ? or # and after the domain, generally. At least for routing.
References
- "Metachondromatosis | Genetic and Rare Diseases Information Center (GARD) – an NCATS Program". rarediseases.info.nih.gov. Retrieved 27 June 2019.
- Kennedy LA (1983). "metachondromatosis". Radiology. 148 (1): 117–8. doi:10.1148/radiology.148.1.6602353. PMID 6602353.
- Sobreira NL, Cirulli ET, Avramopoulos D, et al. (2010). "Whole-genome sequencing of a single proband together with linkage analysis identifies a Mendelian disease gene". PLoS Genet. 6 (6): e1000991. doi:10.1371/journal.pgen.1000991. PMC 2887469. PMID 20577567.
- Hunter AG, Kozlowski K, Hochberger O (1995). "Metachondromatosis". Can Assoc Radiol J. 46 (3): 202–8. PMID 7538882.
External links
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External resources |
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