Treatment of a Prader-Willi Patient with Recurrent Catatonia
Prader-Willi is a genetic disorder characterized by neonatal hypotonia, hyperphagia, short stature, hypogonadism, and mental delay. This disorder can result from multiple mechanisms, most commonly a deletion of paternal chromosome 15, leaving a single maternally derived chromosome 15. Individuals wh...
Saved in:
| Main Authors: | Hana M. Poser, Alexandru E. Trutia |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
Wiley
2015-01-01
|
| Series: | Case Reports in Psychiatry |
| Online Access: | http://dx.doi.org/10.1155/2015/697428 |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Prader-Willi Syndrome in Neonates
by: J Gordon Millichap
Published: (1990-12-01) -
Prader-Willi Syndrome. About a Case
by: Carlos Enrique Cruz Carrazana, et al.
Published: (2021-04-01) -
Dermatilomanía y síndrome de Prader-Willi
by: Lucy García, et al.
Published: (2019-02-01) -
Adult Prader-Willi Syndrome: An Update on Management
by: Luk Ho-Ming
Published: (2016-01-01) -
Management of Hyperphagia and Obesity in Prader–Willi
Syndrome
by: JiHoon Hwang, et al.
Published: (2023-12-01)