Kallmann's syndrome and normosmic isolated hypogonadotropic hypogonadism: two largely overlapping manifestations of one rare disorder

J Endocrinol Invest. 2014 May;37(5):499-500. doi: 10.1007/s40618-014-0063-z. Epub 2014 Apr 9.
No abstract available

Publication types

  • Letter
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Diagnosis, Differential
  • Gonadotropin-Releasing Hormone / deficiency
  • Gonadotropin-Releasing Hormone / genetics
  • Humans
  • Hypogonadism / diagnosis
  • Hypogonadism / etiology
  • Hypogonadism / genetics
  • Hypogonadism / physiopathology*
  • Kallmann Syndrome / diagnosis
  • Kallmann Syndrome / etiology
  • Kallmann Syndrome / genetics
  • Kallmann Syndrome / physiopathology*
  • Mutation
  • Olfaction Disorders / etiology
  • Olfactory Nerve Diseases / etiology
  • Polymorphism, Single Nucleotide

Substances

  • Gonadotropin-Releasing Hormone

Supplementary concepts

  • Hypogonadotropic hypogonadism and anosmia, autosomal dominant
  • Idiopathic Hypogonadotropic Hypogonadism