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Trehalase Deficiency

Also Known As:

Trehalose Intolerance

Networked: 8 relevant articles (0 outcomes, 1 trials/studies)

Disease Context: Research Results

Related Diseases

1.	Glucose-Galactose Malabsorption
2.	Congenital Lactase Deficiency
3.	congenital Sucrase-isomaltase deficiency

Experts

1.	Balanovska, E V: 1 article (01/2021)
2.	Balanovsky, O P: 1 article (01/2021)
3.	Gorin, I O: 1 article (01/2021)
4.	Kozlov, A I: 1 article (01/2021)
5.	Lavryashina, M B: 1 article (01/2021)
6.	Vershubskaya, G G: 1 article (01/2021)
7.	Gallo, A: 1 article (01/2013)
8.	Gasbarrini, A: 1 article (01/2013)
9.	Montalto, M: 1 article (01/2013)
10.	Ojetti, V: 1 article (01/2013)

Drugs and Biologics

Drugs and Important Biological Agents (IBA) related to Trehalase Deficiency:

1.	TrehaloseIBA 01/01/2013 - "Trehalose malabsorption due to trehalase deficiency represents a very rare condition and available studies do not support its relevance in clinical practice. "
2.	LactaseIBA 01/01/1977 - "Enterokinase, lactase, sucrase and trehalase deficiency can be diagnosed by histochemical methods. " 06/01/1989 - "Isolated forms of enzyme deficiencies other than lactase deficiency, such as sucrase-isomaltase or trehalase deficiency were not present among 168 investigations carried out from 1972-1982. "
3.	Sucrase (Sucrose alpha-D-Glucohydrolase)IBA 01/01/1977 - "Enterokinase, lactase, sucrase and trehalase deficiency can be diagnosed by histochemical methods. " 06/01/1989 - "Isolated forms of enzyme deficiencies other than lactase deficiency, such as sucrase-isomaltase or trehalase deficiency were not present among 168 investigations carried out from 1972-1982. "
4.	EnzymesIBA 06/01/1989 - "Isolated forms of enzyme deficiencies other than lactase deficiency, such as sucrase-isomaltase or trehalase deficiency were not present among 168 investigations carried out from 1972-1982. " 06/01/1977 - "Primary carbohydrate (CH) intolerance is characterized by the congenital or acquired absence of individual brush border enzymes or of monosaccharide "carriers" without morphologic abnormalities of the intestinal villus: lactose, sucrose and trehalose intolerance and glucose-galactose malabsorption (brush border diseases). "
5.	DisaccharidasesIBA 01/01/2008 - "Only 4 patients (2%) presented selective alpha,alpha-trehalase deficiency with otherwise normal disaccharidases. " 11/01/2022 - "There are currently three known congenital disaccharidase deficiencies: congenital lactase deficiency (CLD), congenital sucrase-isomaltase deficiency (CSD), and congenital trehalase deficiency (CTD). "
6.	TrehalaseIBA 03/01/2000 - "The normal range of trehalase activity and the incidence of isolated trehalase deficiency in the UK have not been reported. "
7.	Sucrose (Saccharose)IBA 06/01/1977 - "Primary carbohydrate (CH) intolerance is characterized by the congenital or acquired absence of individual brush border enzymes or of monosaccharide "carriers" without morphologic abnormalities of the intestinal villus: lactose, sucrose and trehalose intolerance and glucose-galactose malabsorption (brush border diseases). "
8.	Oligo-1,6-Glucosidase (Isomaltase)IBA 06/01/1989 - "Isolated forms of enzyme deficiencies other than lactase deficiency, such as sucrase-isomaltase or trehalase deficiency were not present among 168 investigations carried out from 1972-1982. "
9.	MonosaccharidesIBA 06/01/1977 - "Primary carbohydrate (CH) intolerance is characterized by the congenital or acquired absence of individual brush border enzymes or of monosaccharide "carriers" without morphologic abnormalities of the intestinal villus: lactose, sucrose and trehalose intolerance and glucose-galactose malabsorption (brush border diseases). "
10.	Lactose FDA LinkGeneric 06/01/1977 - "Primary carbohydrate (CH) intolerance is characterized by the congenital or acquired absence of individual brush border enzymes or of monosaccharide "carriers" without morphologic abnormalities of the intestinal villus: lactose, sucrose and trehalose intolerance and glucose-galactose malabsorption (brush border diseases). "

Therapies and Procedures

1.	Oral Administration 01/01/2008 - "Our data suggest that alpha,alpha-trehalase deficiency is more common than is believed and that oral administration of S. "