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What is another word for Hyperostosis Cortical Congenital?

Pronunciation: [hˌa͡ɪpəɹəstˈə͡ʊsɪs kˈɔːtɪkə͡l kənd͡ʒˈɛnɪtə͡l] (IPA)

Hyperostosis cortical congenital, also known as Caffey disease, is a rare genetic disorder that affects bone development in infants. The condition is characterized by abnormal thickening of the bones, especially in the long bones of the legs and arms. While "hyperostosis cortical congenital" is the medical term commonly used to describe this disease, there are synonyms that can also be applied. These include Caffey syndrome, infantile cortical hyperostosis, and hereditary hyperostosis corticalis generalisata. Though the names may differ, the symptoms and effects of this condition remain the same. Prompt diagnosis and appropriate management are crucial to ensure the best possible outcomes for affected individuals.
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What are the opposite words for Hyperostosis Cortical Congenital?

Hyperostosis Cortical Congenital, also known as Caffey's disease, is a rare genetic condition that causes abnormal bone growth and inflammation. There are no exact antonyms for this term as it is a specific medical condition. However, some terms that could be considered opposites in the context of bone health and abnormalities include osteoporosis, osteomalacia, and osteogenesis imperfecta. Osteoporosis is a condition where bones become weak and brittle, while osteomalacia is a disease characterized by soft bones due to a lack of minerals like calcium and vitamin D. Osteogenesis imperfecta is a genetic disorder that causes bones to be brittle and break easily.

What are the antonyms for Hyperostosis cortical congenital?

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