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What is another word for Infantile Form Sialuria?

Pronunciation: [ˈɪnfəntˌa͡ɪl fˈɔːm sˌa͡ɪəlˈʊ͡əɹi͡ə] (IPA)

Infantile Form Sialuria is a rare metabolic disorder characterized by the deficiency of an enzyme called N-acetylneuraminic acid lyase. This condition affects the body's ability to break down certain complex sugars, leading to the accumulation of substances called sialic acids. While there are no exact synonyms for the term "Infantile Form Sialuria", it can be referred to as Salla disease, as it is one of the two clinical forms of the disorder. Other terms that may be associated with this condition are N-acetylneuraminic acid storage disease or free sialic acid storage disorder. Although these names do not have the exact same meaning, they all encompass the same metabolic disorder known as Infantile Form Sialuria.
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What are the opposite words for Infantile Form Sialuria?

Infantile form sialuria is a rare genetic disorder that affects the metabolism of sialic acid. It is characterized by various symptoms such as intellectual disability, difficulty in speech, abnormal bone development, and other physical and mental abnormalities. Therefore, the antonyms that can be used for infantile form sialuria are health, development, intellect, speech, normalcy, and stability. Additionally, the disease can be countered by early detection, proper medical care, physical therapy, and nutritional support. Nevertheless, researchers are continuously studying this illness to develop new treatment options, so affected individuals can lead a better quality of life.

What are the antonyms for Infantile form sialuria?

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