dysostosis multiplex (Meaning)

Wordnet

dysostosis multiplex (n)

hereditary disease (autosomal recessive) consisting of an error is mucopolysaccharide metabolism; characterized by severe abnormalities in development of skeletal cartilage and bone and mental retardation

Synonyms & Antonyms of dysostosis multiplex

No Synonyms and anytonyms found

dysostosis multiplex Sentence Examples

  1. Dysostosis multiplex is a rare genetic disorder that primarily affects bone and cartilage development.
  2. Individuals with dysostosis multiplex may have multiple skeletal abnormalities, including shortened limbs, joint deformities, and an abnormal rib cage.
  3. The underlying cause of dysostosis multiplex is a mutation in the COL11A2 gene, which provides instructions for making a protein that is essential for the formation of cartilage and bone.
  4. Dysostosis multiplex can be diagnosed through a combination of physical examination, X-rays, and genetic testing.
  5. There is no cure for dysostosis multiplex, but treatment options can help manage the symptoms and improve quality of life.
  6. Treatment for dysostosis multiplex may include physical therapy, occupational therapy, medications, and surgical interventions.
  7. Individuals with dysostosis multiplex may experience challenges with mobility, pain, and respiratory problems.
  8. Dysostosis multiplex can lead to an increased risk of fractures, joint dislocations, and other complications.
  9. People with dysostosis multiplex often have difficulty with everyday tasks, such as walking, climbing stairs, and lifting objects.
  10. Dysostosis multiplex is a complex and challenging condition, but with proper care and support, individuals with this disorder can live full and active lives.

FAQs About the word dysostosis multiplex

hereditary disease (autosomal recessive) consisting of an error is mucopolysaccharide metabolism; characterized by severe abnormalities in development of skelet

No synonyms found.

No antonyms found.

Dysostosis multiplex is a rare genetic disorder that primarily affects bone and cartilage development.

Individuals with dysostosis multiplex may have multiple skeletal abnormalities, including shortened limbs, joint deformities, and an abnormal rib cage.

The underlying cause of dysostosis multiplex is a mutation in the COL11A2 gene, which provides instructions for making a protein that is essential for the formation of cartilage and bone.

Dysostosis multiplex can be diagnosed through a combination of physical examination, X-rays, and genetic testing.