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From Feeding Challenges to Oral-Motor Dyspraxia: A Comprehensive Description of 10 New Cases with CTNNB1 Syndrome.
Onesimo, Roberta; Sforza, Elisabetta; Trevisan, Valentina; Leoni, Chiara; Giorgio, Valentina; Rigante, Donato; Kuczynska, Eliza Maria; Proli, Francesco; Agazzi, Cristiana; Limongelli, Domenico; Digilio, Maria Cistina; Dentici, Maria Lisa; Macchiaiolo, Maria; Novelli, Antonio; Bartuli, Andrea; Sinibaldi, Lorenzo; Tartaglia, Marco; Zampino, Giuseppe.
Afiliação
  • Onesimo R; Center for Rare Diseases and Birth Defects, Department of Woman and Child Health and Public Health, Fondazione Policlinico Universitario A. Gemelli IRCCS, 00168 Roma, Italy.
  • Sforza E; Department of Life Sciences and Public Health, Faculty of Medicine and Surgery, Università Cattolica del Sacro Cuore, 00168 Roma, Italy.
  • Trevisan V; Center for Rare Diseases and Birth Defects, Department of Woman and Child Health and Public Health, Fondazione Policlinico Universitario A. Gemelli IRCCS, 00168 Roma, Italy.
  • Leoni C; Center for Rare Diseases and Birth Defects, Department of Woman and Child Health and Public Health, Fondazione Policlinico Universitario A. Gemelli IRCCS, 00168 Roma, Italy.
  • Giorgio V; Center for Rare Diseases and Birth Defects, Department of Woman and Child Health and Public Health, Fondazione Policlinico Universitario A. Gemelli IRCCS, 00168 Roma, Italy.
  • Rigante D; Center for Rare Diseases and Birth Defects, Department of Woman and Child Health and Public Health, Fondazione Policlinico Universitario A. Gemelli IRCCS, 00168 Roma, Italy.
  • Kuczynska EM; Department of Life Sciences and Public Health, Faculty of Medicine and Surgery, Università Cattolica del Sacro Cuore, 00168 Roma, Italy.
  • Proli F; Center for Rare Diseases and Birth Defects, Department of Woman and Child Health and Public Health, Fondazione Policlinico Universitario A. Gemelli IRCCS, 00168 Roma, Italy.
  • Agazzi C; Center for Rare Diseases and Birth Defects, Department of Woman and Child Health and Public Health, Fondazione Policlinico Universitario A. Gemelli IRCCS, 00168 Roma, Italy.
  • Limongelli D; Department of Life Sciences and Public Health, Faculty of Medicine and Surgery, Università Cattolica del Sacro Cuore, 00168 Roma, Italy.
  • Digilio MC; Department of Life Sciences and Public Health, Faculty of Medicine and Surgery, Università Cattolica del Sacro Cuore, 00168 Roma, Italy.
  • Dentici ML; Medical Genetics Unit, IRCCS Bambino Gesù Children Hospital, 00168 Roma, Italy.
  • Macchiaiolo M; Medical Genetics Unit, IRCCS Bambino Gesù Children Hospital, 00168 Roma, Italy.
  • Novelli A; Medical Genetics Unit, IRCCS Bambino Gesù Children Hospital, 00168 Roma, Italy.
  • Bartuli A; Medical Genetics Unit, IRCCS Bambino Gesù Children Hospital, 00168 Roma, Italy.
  • Sinibaldi L; Medical Genetics Unit, IRCCS Bambino Gesù Children Hospital, 00168 Roma, Italy.
  • Tartaglia M; Medical Genetics Unit, IRCCS Bambino Gesù Children Hospital, 00168 Roma, Italy.
  • Zampino G; Molecular Genetics and Functional Genomics Unit, IRCCS Bambino Gesù Children's Hospital, 00146 Roma, Italy.
Genes (Basel) ; 14(10)2023 09 22.
Article em En | MEDLINE | ID: mdl-37895192
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Apraxias / Sialorreia / Transtornos do Neurodesenvolvimento / Deficiência Intelectual Limite: Child / Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Apraxias / Sialorreia / Transtornos do Neurodesenvolvimento / Deficiência Intelectual Limite: Child / Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article