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https://www.um.edu.mt/library/oar/handle/123456789/10559| Title: | Prader-Willi syndrome |
| Authors: | Zammit, Lara Maria Vella Baldacchino, Mikhail |
| Keywords: | Prader-Willi syndrome -- Malta -- Case studies |
| Issue Date: | 2013 |
| Publisher: | MMSA |
| Citation: | Minima Medicamenta. 2013, (2), p 125-133 |
| Abstract: | Case regarding a three-year old girl, suffering from Prader-Willi Syndrome, a rare genetic disorder with characteristic, easily recognisable dysmorphic features. She was seen at Children’s Out-patients as part of a follow-up regimen, performed every three months. This consultation was held on the 3rd October, 2012 and another one was planned for the 5th of January, 2013. The clinical picture of developmental signs and symptoms are very characteristic and early diagnosis is beneficial for the anticipation of complications, reduction in unnecessary investigations and improved prognosis. |
| URI: | https://www.um.edu.mt/library/oar//handle/123456789/10559 |
| Appears in Collections: | Minima Medicamenta 2013 Minima Medicamenta 2013 |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| Prader-Willi Syndrome.pdf | 375.83 kB | Adobe PDF | View/Open |
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