Health / Medical Topics |
Galactosemia
An autosomal recessive inherited metabolic disorder caused by mutations in the GALE, GALK1, and GALT genes. It is characterized by deficiency of the enzymes responsible for the metabolism of galactose. Signs and symptoms include intellectual disability, hepatomegaly, hepatic failure, and renal failure. (NCI Thesaurus)
YOU MAY ALSO LIKE
The measurement of the galactose-1-phosphate uridyltransferase in a biologic specimen.
The measurement of the amount of galactose in a biologic specimen.
A hexose which is almost identical to glucose except that orientation of -H and -OH on carbon 4 are exchanged, making it…
Abnormal milky discharge from the nipple.
A carbohydrate polymer composed of mannose and galactose, with chemotherapeutic enhancing activity. Galactomannan derivative binds to galectins on cell surfaces and may…
A procedure that uses x-rays to create pictures of milk ducts in the breast. A very thin catheter (tube) is inserted into…