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What is another word for Infantile Gaucher Disease?

Pronunciation: [ˈɪnfəntˌa͡ɪl ɡˈɔːt͡ʃə dɪzˈiːz] (IPA)

Infantile Gaucher Disease, also known as Type 2 Gaucher Disease, is a rare genetic disorder characterized by a deficiency of an enzyme called glucocerebrosidase. This enzyme is responsible for breaking down a fatty substance called glucocerebroside in the body's cells. Without this enzyme, glucocerebroside accumulates in various organs, leading to severe health complications. Synonyms for Infantile Gaucher Disease include Type 2 Gaucher Disease, Gaucher's Disease Type 2, and Gaucher's Type II. Furthermore, it is sometimes referred to as Severe Gaucher Disease or Acute Neuronopathic Gaucher Disease, indicating the profound neurological involvement associated with this form of Gaucher Disease. Although these terms are interchangeable, they all describe the same devastating condition that affects young children. Early diagnosis and proper management are crucial in providing the best possible care for infants with this progressive and life-threatening disorder.
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What are the opposite words for Infantile Gaucher Disease?

Infantile Gaucher Disease is a rare genetic disorder that affects infants and young children. The disease is caused by the deficiency of an enzyme that helps in breaking down a type of fat in the body. This leads to a buildup of fatty substances in different organs of the body, causing damage to them. There are no antonyms for the disease as it is a medical condition with specific symptoms and treatments. However, some of the antonyms for infantile include mature, grown, adult, and elderly. These words signify the opposite of the childlike state that is characteristic of infants and young children.

What are the antonyms for Infantile gaucher disease?

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