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What is achondroplasia?

Updated: 9/7/2023
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10y ago

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Achondroplasia is characterized by abnormal bone growth that results in short stature with disproportionately short arms and legs, a large head, and characteristic facial features with frontal bossing and mid-face hypoplasia.

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15y ago
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10y ago

Achondroplasia is a genetic disorder that results in abnormal bone growth, short stature and short limbs.

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9y ago

Achondroplasia dwarfism is a mutation in the human body. People with this condition have a short stature and is caused by a change in the gene receptors.

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Q: What is achondroplasia?
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Related questions

How much is medicines or hospitals for people with achondroplasia?

There are no medications for achondroplasia


How is achondroplasia diagnosed?

whats the name of the test that diagnoses achondroplasia


Do Ellie Simmonds parents have achondroplasia?

no Ellie Simmonds parents has not got achondroplasia


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


What is the heredity cause for achondroplasia?

Mutations in the FGFR3 gene are the cause for achondroplasia (short-limbed dwarfism).


Can you get achondroplasia with out having a parent that has it?

Yes People with achondroplasia can be born to parents that do not have the condition. This is the result of a new mutation.[2]


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 was achondroplasia named?

ByPierre Maroteaux


Who was achondroplasia discovered by?

your mom and i in bed


How can you get Achondroplasia?

Achondroplasia, or Dwarfism, is a genetic disorder, both handed down and mutagenic. Quoted from Wikipedia: "Achondroplasia is a result of an autosomal dominant mutation in the fibroplast growth receptor gene 3 (FGFR3), which causes an abnormality of catilage formation."