We report the case of a young male who presented at the age of 34 years with intracranial hemorrhage due to moyamoya disease. He was later diagnosed with hypogonadism and hypopituitarism. Chromosomal evaluation revealed a normal karyotype. The results of further neuroradiological studies led to the diagnosis of empty sella syndrome.

Original languageEnglish
Pages (from-to)472-474
Number of pages3
JournalJournal of Clinical Neuroscience
Issue number4
Publication statusPublished - May 2005


  • Empty sella syndrome
  • Hypogonadism
  • Hypopituitarism
  • Moyamoya disease

ASJC Scopus subject areas

  • Clinical Neurology
  • Neurology
  • Physiology (medical)
  • Surgery


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