Abstract
Four siblings with classic Bardet-Biedl syndrome were studied. The brother had hypogonadism of testicular origin, with high gonadotropin levels and exaggerated responses to luteinizing-hormone-releasing hormone, whereas the 3 sisters showed a normal hypothalamic-pituitary-gonadal axis. The remaining pituitary hormone function was intact.
| Original language | English |
|---|---|
| Pages (from-to) | 514-518 |
| Number of pages | 5 |
| Journal | Israel Journal of Medical Sciences |
| Volume | 16 |
| Issue number | 7 |
| State | Published - 1980 |
| Externally published | Yes |