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What is another word for Neonatal Canavan Disease?

Pronunciation: [nˈiːə͡ʊnˌe͡ɪtə͡l kˈanɐvˌan dɪzˈiːz] (IPA)

Neonatal Canavan Disease is a rare genetic disorder that affects infants, specifically those under six months of age. This condition is characterized by the absence of a certain enzyme in the brain, leading to the build-up of harmful substances that damage nerve cells. Although there are no direct synonyms for Neonatal Canavan Disease, it falls under the broader category of leukodystrophies, a group of genetic disorders affecting the white matter of the brain. Other terms used to describe this condition include Canavan-Van Bogaert-Bertrand Disease, Aspartoacylase deficiency, and Spongy degeneration of childhood. Early diagnosis and management are crucial for affected infants to ensure the best possible outcome and quality of life.
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What are the opposite words for Neonatal Canavan Disease?

Antonyms for Neonatal Canavan Disease include healthy, normal, thriving, and functional. Neonatal Canavan Disease is a rare and severe genetic disorder that affects the development of the brain and nervous system. It leads to a progressive deterioration of motor and cognitive abilities, resulting in severe disability and a shortened lifespan. Antonyms for this condition describe a state of well-being and functioning, with no limitations or impairments. While there is no known cure for Neonatal Canavan Disease, early detection and treatment can improve the quality of life for affected individuals and their families. With ongoing research and advancements in genetic therapies, there is hope for a future without the devastating effects of this rare disease.

What are the antonyms for Neonatal canavan disease?

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