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Achondroplasia is primarily caused by a genetic mutation in the FGFR3 gene and is mostly inherited in an autosomal dominant manner. The most significant risk factor is advanced paternal age, as older fathers are more likely to pass on the mutation. Additionally, having a family history of achondroplasia increases the risk of having affected children. Environmental factors do not play a significant role in the development of this condition.
What else can I help you with?
What is the name of the gene for Achondroplasia?
Achondroplasia is caused by a mutation of the fibroblast growth factor receptor 3 (FGFR3) gene.
How does Achondroplasia affect children?
achondroplasia have a very high risk of serious and repeated middle ear infections, which can result in hearing loss. The disease does not affect either mental capacity, or reproductive ability.
What is a synonym for risk factor?
risk factor
When was achondroplasia discovered?
In 1994 Dr. John Wasmuth and his colleagues discovered that a mutation of the fibroblast growth factor receptor-3 (FGFR3) gene on human chromosome 4 causes achondroplasia.
How is achondroplasia diagnosed?
whats the name of the test that diagnoses achondroplasia
How much is medicines or hospitals for people with achondroplasia?
There are no medications for achondroplasia
What is a risk factor to the muscular system?
what is the risk factor of the muscular system
Do Ellie Simmonds parents have achondroplasia?
no Ellie Simmonds parents has not got achondroplasia
Anything that increases the chance of disease or injury?
A risk factor.
Is achondroplasia hereditary?
yes, achondroplasia is hereditary and if one of a parent has it you have 50% chance to inheriting it.
Is there a cure for achondroplasia?
No
Is anyone looking for a cure for achondroplasia?
Yes ,we are looking for a cure for achondroplasia. Please help! Amita
