eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | prader willi syndrome |
| Comorbidity | C0020619|hypogonadism |
| Sentences | 6 |
| PubMedID- 22188746 | Context: the pathophysiology of hypogonadism in boys 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. |
| PubMedID- 22723315 | Context: the etiology of hypogonadism in girls with prader-willi syndrome (pws) remains uncertain. |
| PubMedID- 19946044 | hypogonadism in females with prader-willi syndrome from infancy to adulthood: variable combinations of a primary gonadal defect and hypothalamic dysfunction. |
| PubMedID- 23183360 | Recent findings: prader willi syndrome is associated with hypogonadism, which does not appear to be affected by treatment with rhgh. |
| 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. |
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