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Increased referrals for congenital hyperinsulinism genetic testing in children with trisomy 21 reflects the high burden of non-genetic risk factors in this group.
Hewat, Thomas I; Laver, Thomas W; Houghton, Jayne A L; Männistö, Jonna M E; Alvi, Sabah; Brearey, Stephen P; Cody, Declan; Dastamani, Antonia; De Los Santos La Torre, Miguel; Murphy, Nuala; Rami-Merhar, Birgit; Wefers, Birgit; Huopio, Hanna; Banerjee, Indraneel; Johnson, Matthew B; Flanagan, Sarah E.
Afiliación
  • Hewat TI; Institute of Biomedical and Clinical Science, University of Exeter Medical School, Exeter, UK.
  • Laver TW; Institute of Biomedical and Clinical Science, University of Exeter Medical School, Exeter, UK.
  • Houghton JAL; Exeter Genomics Laboratory, Royal Devon and Exeter NHS Foundation Trust, Exeter, UK.
  • Männistö JME; Department of Pediatrics, University of Eastern Finland and Kuopio University Hospital, Kuopio, Finland.
  • Alvi S; Leeds Children's Hospital, Leeds, UK.
  • Brearey SP; Countess of Chester Hospital, Chester, UK.
  • Cody D; Children's Health Ireland at Crumlin, Dublin, Ireland.
  • Dastamani A; Endocrinology Department, Great Ormond Street Hospital for Children NHS Foundation Trust, London, UK.
  • De Los Santos La Torre M; Department of Endocrinology and Metabolism of the Instituto Nacional de Salud del Niño, Lima, Peru.
  • Murphy N; Children's University Hospital, Dublin, Ireland.
  • Rami-Merhar B; Department of Pediatric and Adolescent Medicine, Medical University of Vienna, Vienna, Austria.
  • Wefers B; Ninewells Hospital, Dundee, UK.
  • Huopio H; Department of Pediatrics, Kuopio University Hospital, Kuopio, Finland.
  • Banerjee I; Department of Paediatric Endocrinology, Royal Manchester Children's Hospital, Manchester, UK.
  • Johnson MB; Institute of Biomedical and Clinical Science, University of Exeter Medical School, Exeter, UK.
  • Flanagan SE; Institute of Biomedical and Clinical Science, University of Exeter Medical School, Exeter, UK.
Pediatr Diabetes ; 23(4): 457-461, 2022 06.
Article en En | MEDLINE | ID: mdl-35294086
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Síndrome de Down / Hiperinsulinismo Congénito Tipo de estudio: Diagnostic_studies / Etiology_studies / Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Pediatr Diabetes Asunto de la revista: ENDOCRINOLOGIA Año: 2022 Tipo del documento: Article País de afiliación: Reino Unido Pais de publicación: Dinamarca
Texto completo
Añadir a Mi BVS
Imprimir
XML
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Síndrome de Down / Hiperinsulinismo Congénito Tipo de estudio: Diagnostic_studies / Etiology_studies / Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Pediatr Diabetes Asunto de la revista: ENDOCRINOLOGIA Año: 2022 Tipo del documento: Article País de afiliación: Reino Unido Pais de publicación: Dinamarca