PedAM
Pediatric Disease Annotations & Medicines
| Disease | prader-willi syndrome |
| Phenotype | C0020619|hypogonadism |
| Sentences | 5 |
| PubMedID- 21718342 | Background: hypogonadism in prader-willi syndrome (pws) is generally attributed to hypothalamic dysfunction or to primary gonadal defect, but pathophysiology is still unclear. |
| PubMedID- 22188746 | Context: the pathophysiology of hypogonadism in boys with prader-willi syndrome (pws) remains uncertain. |
| PubMedID- 19946044 | Objective: the variable hypogonadism in prader-willi syndrome (pws) has generally been attributed to hypothalamic dysfunction. |
| PubMedID- 22723315 | Context: the etiology of hypogonadism in girls with prader-willi syndrome (pws) remains uncertain. |
| PubMedID- 21543378 | In humans, necdin plays a potential role in the hypogonadotropic hypogonadism phenotype in patients with prader-willi syndrome. |
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