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1.
Andes Pediatr ; 92(3): 359-366, 2021 Jun.
Artículo en Inglés, Español | MEDLINE | ID: mdl-34479241

RESUMEN

INTRODUCTION: Prader-Willi Syndrome (PWS) is the most common cause of genetic obesity. Hyperphagia and obe sity are the most associated concepts with this condition. However, undernutrition secondary to severe hypotonia and feeding difficulties is the predominant initial feature. OBJECTIVE: to reprodu ce and communicate the nutritional phases on a series of Chilean cases with PWS. PATIENTS AND METHOD: Cross-sectional study in which clinical records of PWS individuals under nutritional con trol at the Clínica Santa María in Santiago, Chile between 2017 and 2018 were analyzed. The anthro pometric references of the World Health Organization were used to carry out the nutritional as sessment. The classification into nutritional phases was according to the Miller criteria. RESULTS: 24 patients from infants to adults were included. All children aged under 9 months were in phase I and had malnutrition or were eutrophic; those between 9 and 25 months were classified in phase 2a; pa tients between 2.1 and 4.5 years were distributed between phases 1 and 2 and 66% were eutrophic; those between 4.5 to 8 years, 80% were in phase 2a and 2b and obesity begins to appear, and patients over 8 years of age, 75% were in phase 3 and all are overweight or obese. There was an association bet ween nutritional phase and age but not between it and nutritional status. CONCLUSIONS: In our series, the nutritional phases described according to age were reproduced according to those internationally described. There was no association between nutritional status and age.


Asunto(s)
Hiperfagia/etiología , Desnutrición/etiología , Obesidad Infantil/etiología , Síndrome de Prader-Willi/fisiopatología , Adolescente , Adulto , Factores de Edad , Niño , Preescolar , Estudios Transversales , Progresión de la Enfermedad , Femenino , Humanos , Hiperfagia/diagnóstico , Lactante , Recién Nacido , Masculino , Desnutrición/diagnóstico , Obesidad Infantil/diagnóstico , Síndrome de Prader-Willi/diagnóstico , Síndrome de Prader-Willi/psicología , Adulto Joven
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