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What is another word for Congenital Cortical Hyperostosis?

Pronunciation: [kənd͡ʒˈɛnɪtə͡l kˈɔːtɪkə͡l hˌa͡ɪpəɹəstˈə͡ʊsɪs] (IPA)

Congenital Cortical Hyperostosis is a rare skeletal disorder that is characterized by excessive bone formation in the cortex, or outer layer, of the bone. This condition, also known as Caffey's disease, primarily affects infants and is usually self-limiting, meaning it resolves on its own over time. Although this disorder can cause pain and swelling in affected areas, it typically does not lead to any long-term health complications. Synonyms for Congenital Cortical Hyperostosis include infantile cortical hyperostosis, Caffey-Vitale syndrome, and benign infantile hyperostosis. While the exact cause of this condition remains unknown, early diagnosis and management can help alleviate symptoms and ensure a healthy outcome for infants affected by it.
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What are the opposite words for Congenital Cortical Hyperostosis?

Congenital cortical hyperostosis (CCH) is a rare genetic disorder that affects bone growth and density. It is characterized by abnormally thick bones, especially in the skull, jaw, collarbone, and pelvis. There are no antonyms for CCH as it is a medical condition and not a common word. However, some medical interventions and treatments can help manage the symptoms of CCH. These may include medications to reduce bone growth, surgery to correct skeletal deformities, and physical therapy to improve mobility and function. Early diagnosis and treatment can prevent complications such as nerve compression or spinal cord injury, which can affect the patient's quality of life.

What are the antonyms for Congenital cortical hyperostosis?

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