A case report: Familial glucocorticoid deficiency associated with familial focal segmental glomerulosclerosis
<p>Abstract</p> <p>Background</p> <p>Familial glucocorticoid deficiency (FGD) is a rare autosomal recessive disorder characterized by isolated glucocorticoid deficiency in the presence of normal plasma renin and aldosterone level. Focal segmental glomerulosclerosis (FSG...
| Main Authors: | , , |
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| Format: | Article |
| Language: | English |
| Published: |
BMC
2012-12-01
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| Series: | BMC Endocrine Disorders |
| Subjects: | |
| Online Access: | http://www.biomedcentral.com/1472-6823/12/32 |