eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | prader willi syndrome |
| Comorbidity | C0028754|obesity |
| Sentences | 5 |
| PubMedID- 22043167 | A prader-willi syndrome-like phenotype with obesity has been described in fragile x syndrome individuals with the cgg expansion mutation [29], indicating that the obesity is probably due to loss of fmr1 function and interaction with other genes. |
| PubMedID- 23135822 | There are additional reasons to suggest that oxytocin may be particularly effective in combating obesity associated with prader-willi syndrome (pws). |
| PubMedID- 20880597 | Background: the muscle hypotonia and obesity associated with prader-willi syndrome (pws) result in a high rate of obstructive sleep apnea (osa). |
| PubMedID- 21345363 | In contrast to other forms of obesity, patients with prader-willi syndrome (pws) display high levels of ghrelin, reduced visceral adiposity and relative hypoinsulinemia. |
| PubMedID- 21632815 | Context: prader-willi syndrome (pws) is associated with hyperphagia and obesity, without effective pharmacological treatment. |
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