Achondroplasia (short-limbed dwarfism) is a genetic disorder that impairs embryonic development, resulting in abnormalities in bone growth and cartilage development.
Achondroplasia can be detected through prenatal screening.
Achondroplasia occurs in all races and with equal frequency in males and females and affects about one in every 40,000 children.
An individual with achondroplasia has disproportionate short stature.
Chiari malformations are found in several known genetic disorders such as achondroplasia, Hadju-Cheney syndrome, and Klippel-Feil syndrome.
In achondroplasia, the long bones fail to develop normally, making the arms and legs disproportionately short and stubby (and sometimes curved).
In some cases physical development may be disproportionate, as in achondroplasia, but in others the parts of the body develop proportionately.
Matt's wife Amy has a type of dwarfism called achondroplasia.
Of these, Achondroplasia is the most common, affecting about 80 percent of all little people.
Persons with achondroplasia are 3-5 feet (91-152 cm) tall and of normal intelligence.
Scenario 2 The patientâs story Clinicianâs response Mrs C is concerned about her son who has achondroplasia.
The actor suffered from achondroplasia, a form of dwarfism.
The four most common causes of dwarfism in children are achondroplasia, Turner syndrome, inadequate pituitary function (pituitary dwarfism), and lack of emotional or physical nurturance.
There is no specific treatment for achondroplasia, besides treating any orthopedic problems that may arise.
Those with achondroplasia seldom reach 5 feet (1.5 m) in height.