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Familial glucocorticoid deficiency
- Familial glucocorticoid deficiency is a condition that occurs when the adrenal glands, which are hormone-producing glands located on top of each kidney, do not ...
- ... the NNT gene have been found to cause familial glucocorticoid deficiency. This condition is characterized by potentially life-threatening ... of other family members (hyperpigmentation). The features of familial glucocorticoid deficiency are caused by an inability of the adrenal ...
- ... the MRAP gene have been found to cause familial glucocorticoid deficiency. This condition is characterized by potentially life-threatening ... functions, leading to the signs and symptoms of familial glucocorticoid deficiency. More About This Health Condition B27 C21orf61 FALP ...
- ... the MC2R gene have been found to cause familial glucocorticoid deficiency. This condition is characterized by potentially life-threatening ... functions, leading to the signs and symptoms of familial glucocorticoid deficiency. More About This Health Condition MedlinePlus Genetics provides ...
- ... insufficiency neurologic disorder Allgrove syndrome Genetic Testing Registry: Glucocorticoid deficiency with achalasia Triple A syndrome National Organization for ...
- ... known as complete 17α-hydroxylase/17,20-lyase deficiency.Without 17α-hydroxylase activity, pregnenolone and progesterone are not converted to 17-hydroxypregnenolone or 17-hydroxyprogesterone, impairing production of glucocorticoids. Instead pregnenolone and progesterone are processed to form ...
- The SERPINA6 gene provides instructions for making a protein called corticosteroid-binding globulin (CBG), which is primarily produced in the liver. The CBG ...