Abstract
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 language | English |
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Pages (from-to) | 472-474 |
Number of pages | 3 |
Journal | Journal of Clinical Neuroscience |
Volume | 12 |
Issue number | 4 |
DOIs | |
Publication status | Published - May 2005 |
Keywords
- Empty sella syndrome
- Hypogonadism
- Hypopituitarism
- Moyamoya disease
ASJC Scopus subject areas
- Clinical Neurology
- Neurology
- Physiology (medical)
- Surgery