Micronutrient in hyperphenylalaninemia.

Fecha de publicación: 01/09/2015

Autores de IIS La Fe

Jaime Dalmau Serra

Autor
Isidro Vitoria Miñana

Autor

Participantes ajenos a IIS La Fe

Crujeiras V
Aldamiz-Echevarria L
Andrade F
Roca I
Leis R
Fermandez-Marmiesse A
Couce ML

Grupos

Nutrición y Metabolopatías

Investigador Principal

Patricia Correcher Medina

Abstract

The data presented here are the biochemical parameters of 156 patients with hyperphenylalaninemia. PKU patients, who, in order to maintain optimal serum Phe concentrations, receive dietary treatment consisting of a diet low in natural protein supplemented with special low protein foods and a Phe-free amino acid mixture, vitamins and minerals. The obtained data reflects a high percentage of patients with prealbumin and selenium deficiencies, as well as an increased level of folic acid. This data article is related to the research article entitled, "Vitamin and mineral status in patients with hyperphenylalaninemia", by Crujeiras et al. [1].

Datos de la publicación

ISSN/ISSNe:: 2352-3409,
Tipo:: Article
Páginas:: 614-621
DOI:: 10.1016/j.dib.2015.07.026
PubMed:: 26322328
Factor de Impacto:: 0,187 SCImago ℠
Cuartil:: Q3 SCImago ℠

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Métricas

Filiaciones

Crujeiras V:: Unit of Gastroenterology and Nutrition, Department of Pediatrics, Hospital Clinico Universitario de Santiago, Travesia da Choupana s/n, 15706 Santiago de Compostela, A Coruna, Spain
Aldamiz-Echevarria L:: Unit of Metabolism, Department of Pediatrics, Hospital de Cruces, Group of Metabolism, Biocruces Health Research Institute, CIBERER, Plaza de Cruces s/n, 48903 Barakaldo, Vizcaya, Spain
Dalmau J:: Unit of Metabolopathies, Hospital Universitario la Fe, Bulevarsur s/n, 46021 Valencia, Spain
Vitoria I:: Unit of Metabolopathies, Hospital Universitario la Fe, Bulevarsur s/n, 46021 Valencia, Spain
Andrade F:: Unit of Metabolism, Department of Pediatrics, Hospital de Cruces, Group of Metabolism, Biocruces Health Research Institute, CIBERER, Plaza de Cruces s/n, 48903 Barakaldo, Vizcaya, Spain
Roca I:: Unit of Diagnosis and Treatment of Congenital Metabolic Diseases, S. Neonatology, Department of Pediatrics, Hospital Clinico Universitario de Santiago, Travesia da Choupana s/n, 15706 Santiago de Compostela, A Coruna, Spain
Leis R:: Unit of Gastroenterology and Nutrition, Department of Pediatrics, Hospital Clinico Universitario de Santiago, Travesia da Choupana s/n, 15706 Santiago de Compostela, A Coruna, Spain
Fermandez-Marmiesse A:: Unit of Diagnosis and Treatment of Congenital Metabolic Diseases, S. Neonatology, Department of Pediatrics, Hospital Clinico Universitario de Santiago, CIBERER, Health Research Institute of Santiago de Compostela (IDIS), Travesia da Choupana s/n, 15706 Santiago de Compostela, A Coruna, Spain
Couce ML:: Unit of Diagnosis and Treatment of Congenital Metabolic Diseases, S. Neonatology, Department of Pediatrics, Hospital Clinico Universitario de Santiago, CIBERER, Health Research Institute of Santiago de Compostela (IDIS), Travesia da Choupana s/n, 15706 Santiago de Compostela, A Coruna, Spain