(PDF) Manejo Hospitalario de Desnutrición Severa en Pediatría
(PDF) Manejo Hospitalario de Desnutrición Severa en Pediatría
Authors:
Ana Gabriela Ayala Germán Alejandro Flora Zárate-Mondragón Erick Manuel Toro-Monjaraz
Instituto Nacional de Pediatría Loredo Instituto Nacional de Pediatría Instituto Nacional de Pediatría
Mayer
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CRITERIO PEDIÁTRICO
Acta Pediatr Mex 2022; 43 (3): 193-201.
pediatría
C
Hospital treatment of pediatric severe malnutrition
Acta Pediatr Mex 2022; 43 (3): 193-201.
Ana Gabriela Ayala-Germán,1a Alejandro Loredo-Ma yer,,2b Flora Zárate-Mondr
Loredo-Mayer
yer agón, 2c Erick Manuel TToro-
Zárate-Mondragón, oro-
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Francisco Roberto
oberto
Download full-text PDF
Cervantes-Bustamante, 3h Download citation
Jaime Alfonso Ramírez-Mayans4i Copy link
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Ana Gabriela Ayala-Germán, Alejandro Loredo-Mayer, Flora Zárate-Mondragón, Erick Manuel Toro-
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Citations (1) References (18)
... Los exámenes de laboratorio a su ingreso: Na+ 128 mmol/L, K+ 2.8 mmol/L, Cl-93 mmol/L, P 4 mmol/L, Mg 2.3
mmol/L, Ca-12.7 mmol/L, glucosa 111 mg/dl, creatinina 0.24 mg/dl, nitrógeno ureico 5.3 mg/dl, gasometría con pH 7.45,
PO 2 Síndrome de kwashiorkor en un lactante. A propósito de un caso Con base en los hallazgos clínicos y de
laboratorio, se sospechó de síndrome de kwashiorkor y se ingresó a piso de Gastroenterología y Nutrición, para
mejorar su condición clínica e iniciar rehabilitación nutricional. ...
Manifestaciones dermatológicas en una lactante con síndrome de kwashiorkor: Claves para el diagnóstico y
tratamiento oportuno
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OBJETIVO: Describir las distintas herramientas de cribado para el diagnóstico de desnutrición intrahospitalaria y comparar sus
diferencias. MATERIAL Y MÉTODO: Estudio comparativo y retrospectivo de búsqueda bibliográfica en las bases de datos Scientific
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swallowing, frequently present in patients with neurological diseases. Nutritional recovery is the objective in these patients evaluating
the nutritional status after the placement of a PEG in the pediatric population. This is a retrospective cohort conducted to ... [Show full
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La galactosemia es un trastorno hereditario del metabolismo de la galactosa causado por una actividad deficiente en una de las
cuatro enzimas de la vía de Leloir. La forma clásica y severa de presentación es la deficiencia de Galactosa-1-fostato uridiltransferasa
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