What is another word for alpha Fucosidase Deficiency Diseases?
Pronunciation: [ˈalfə fjˈuːkəsˌɪde͡ɪs dɪfˈɪʃənsi dɪzˈiːzɪz] (IPA) 
Alpha fucosidase deficiency diseases, also known as alpha fucosidosis, are a group of rare and inherited metabolic disorders. These conditions result from a deficiency of the enzyme alpha fucosidase, which plays a crucial role in breaking down complex molecules within cells. Alpha fucosidase deficiency can lead to the accumulation of harmful substances in various tissues and organs, causing progressive deterioration of multiple systems in the body.
Synonyms for alpha fucosidase deficiency diseases include fucosidosis, alpha-L-fucosidase deficiency, and fucosidase alpha-L-1 deficiency. Alpha fucosidosis is a term commonly used to describe this set of disorders, emphasizing the deficiency in the enzyme alpha fucosidase. Individuals with these conditions experience a range of symptoms, such as developmental delays, intellectual disabilities, skeletal abnormalities, respiratory issues, and hepatosplenomegaly
