achondroplasia
noun
achon·dro·pla·sia
ˌā-ˌkän-drə-ˈplā-zh(ē-)ə 
: a genetic disorder that is marked by abnormally slow conversion of cartilage to bone during development resulting in a form of dwarfism characterized by a usually normal torso and shortened limbs and that is usually inherited as an autosomal dominant trait
Examples of achondroplasia in a Sentence
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On Tuesday's episode of Little People, Big World, Tori Roloff opened up about how learning of baby Lilah's achondroplasia.
—
Amanda Garrity, Good Housekeeping, 8 Apr. 2020
As a person with achondroplasia, the most common form of dwarfism, dating can be kind of tough when a lot of people are looking for that six-foot-four guy.
—Taylor Lorenz, New York Times, 18 Mar. 2020
Vosoritide is a daily injection meant to counteract the genetic mutation that causes achondroplasia.
—Damian Garde, STAT, 16 Dec. 2019
Bayles was born with achondroplasia, a genetic order that results in dwarfism.
—NBC News, 21 Feb. 2020
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Amanda Garrity, Good Housekeeping, 8 Apr. 2020
As a person with achondroplasia, the most common form of dwarfism, dating can be kind of tough when a lot of people are looking for that six-foot-four guy.
—Taylor Lorenz, New York Times, 18 Mar. 2020
Vosoritide is a daily injection meant to counteract the genetic mutation that causes achondroplasia.
—Damian Garde, STAT, 16 Dec. 2019
Bayles was born with achondroplasia, a genetic order that results in dwarfism.
—NBC News, 21 Feb. 2020
See all Example Sentences for achondroplasia
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Cite this Entry
“Achondroplasia.” Merriam-Webster.com Dictionary, Merriam-Webster, https://www.merriam-webster.com/dictionary/achondroplasia. Accessed 22 Nov. 2024.
Copy CitationMedical Definition
achondroplasia
noun
achon·dro·pla·sia
ˌā-ˌkän-drə-ˈplā-zh(ē-)ə
: a genetic disorder that is marked by abnormally slow conversion of cartilage to bone during development and results in a form of dwarfism characterized by a usually normal torso and shortened limbs
Note: Achondroplasia is usually inherited as an autosomal dominant trait requiring that only one parent passes on a copy of the defective gene on a chromosome other than a sex chromosome. The majority of cases of achondroplasia result from a new spontaneous gene mutation.
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