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What is another word for Cortical Congenital Hyperostosis?

Pronunciation: [kˈɔːtɪkə͡l kənd͡ʒˈɛnɪtə͡l hˌa͡ɪpəɹəstˈə͡ʊsɪs] (IPA)

Cortical Congenital Hyperostosis, also known as Caffey disease or infantile cortical hyperostosis, is a rare genetic condition that affects the bones in infants. This disorder leads to excessive bone growth and thickening, mainly in the outer layer of the bones called the cortex. Although a complex medical term, there are synonymous phrases or alternative names used to describe this condition. Some of these include Infantile Cortical Hyperostosis and Caffey Syndrome. Understanding the variety of terms associated with Cortical Congenital Hyperostosis can aid in effective communication between healthcare professionals, patients, and families affected by this rare genetic disorder.
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What are the opposite words for Cortical Congenital Hyperostosis?

Cortical Congenital Hyperostosis, also known as van Buchem disease, is a rare genetic condition that causes excessive bone growth, particularly in the skull and facial bones. While there are no true antonyms for this condition, treatments aim to manage and slow down the abnormal bone growth. Some of the management techniques include using bisphosphonates, which inhibit bone resorption, and surgery to relieve pressure on the brain caused by the excessive bone growth. Additionally, physical therapy can help to maintain joint mobility and reduce pain associated with this condition. While there are no direct opposites for cortical congenital hyperostosis, these treatments aim to balance or reverse the effects of the disease.

What are the antonyms for Cortical congenital hyperostosis?

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