No direct relationship has been found between inherited metabolic disorders and maternal gestational glucose. Inherited metabolic diseases are genetic disorders caused by defects in metabolic function, most of which are monogenic, and are generally thought to be associated with genetic defects in the biosynthesis of certain enzymes, carriers, receptors, and membrane pumps composed of proteins or (and) polypeptides that are necessary for the maintenance of normal metabolism in the body. A series of physiological changes may occur during pregnancy, resulting in an increased demand for glucose. However, increased insulin resistance and relatively insufficient insulin secretion may induce gestational diabetes mellitus, which, if treated appropriately and maintained at a stable level of glycemia, does not have any significant adverse effects on either the mother or the fetus. However, poor glycemic control can lead to neonatal hypoglycemia, neonatal respiratory distress syndrome, neonatal erythrocytosis, neonatal hyperbilirubinemia, and other diseases. Patients diagnosed with inherited metabolic disorders should actively cooperate with doctors for treatment. If you are not sure about the relationship between inherited metabolic disorders and maternal gestational blood glucose, you can go to the hospital and consult a specialized doctor.