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  3. Research By Disease

Disease: Familial hypersecretion of adrenal androgens

  • Adrenocortical carcinoma: an ominous cause of hirsutism
  • Androgen producing adrenal adenoma. Report on a case associated with hyperparathyroidism
  • COMETE, a network for the study and management of hypersecreting adrenal tumors
  • Elevated Serum Androstenedione Level in a Patient With Ectopic Adrenocorticotropic Hormone Syndrome
  • Familial hypersecretion of adrenal androgens transmitted as a dominant, non-HLA linked trait
  • Formulation and noncontraceptive uses of the new, low-dose oral contraceptive
  • Glucocorticoid resistance syndrome: A diagnostic and therapeutic approach
  • Identification of non-amplifying CYP21 genes when using PCR-based diagnosis of 21-hydroxylase deficiency in congenital adrenal hyperplasia (CAH) affected pedigrees
  • Primary Generalized Glucocorticoid Resistance Syndrome
  • Testicular leydig cell hyperplasia as a cause of familial sexual precocity
  • Venous sampling can be crucial in identifying the testicular origin of idiopathic male luteinising hormone-independent sexual precocity
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About CheckOrphan

CheckOrphan is a non-profit organization located in Basel, Switzerland and Santa Cruz, California that is dedicated to rare, orphan and neglected diseases. CheckOrphan offers users an interactive and dynamic platform for all these diseases. This strategy allows visitors to be updated daily on all the latest news and interact with people internationally. This is essential, because due to the nature of these diseases, there is not a large concentration of individuals within any given proximity.
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