AI Article Synopsis
- Cleidocranial dysplasia (CCD) is a rare genetic disorder that is inherited in an autosomal dominant manner, causing issues with the skull, shoulders, teeth, spine, and face.
- Individuals with CCD experience different levels of impairment, affecting their physical appearance and function.
- Early detection and appropriate treatment are crucial for reducing complications, assisting in family planning, and improving overall quality of life for those affected.
Article Abstract
Cleidocranial dysplasia (CCD) is a rare autosomal dominant disorder with facial, dental, and skeletal impairments. Affected individuals have varying degrees of skull, shoulder, dental, spine, and facial impairments. Early diagnosis and timely intervention help in minimization of complications, planning of pregnancy, and better quality of life.
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Source |
|---|---|
| http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9547988 | PMC |
| http://dx.doi.org/10.1002/ccr3.6440 | DOI Listing |
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