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Hyperphosphatemic familial tumoral calcinosis secondary to fibroblast growth factor 23 (FGF23) mutation: a report of two affected families and review of the literature.
Chakhtoura, M; Ramnitz, M S; Khoury, N; Nemer, G; Shabb, N; Abchee, A; Berberi, A; Hourani, M; Collins, M; Ichikawa, S; El Hajj Fuleihan, G.
Afiliação
  • Chakhtoura M; Calcium Metabolism and Osteoporosis Program, WHO Collaborating Center for Metabolic Bone Disorders, American University of Beirut Medical Center, Beirut, Lebanon. mc39@aub.edu.lb.
  • Ramnitz MS; Section on Skeletal Disorders and Mineral Homeostasis, National Institute of Dental and Craniofacial Research, National Institutes of Health, Bethesda, MD, USA.
  • Khoury N; Department of Radiology, American University of Beirut Medical Center, Beirut, Lebanon.
  • Nemer G; Department of Biochemistry and Molecular Genetics, American University of Beirut Medical Center, Beirut, Lebanon.
  • Shabb N; Department of Pathology and Laboratory Medicine, American University of Beirut Medical Center, Beirut, Lebanon.
  • Abchee A; Department of Internal Medicine, American University of Beirut Medical Center, Beirut, Lebanon.
  • Berberi A; Department of Internal Medicine, American University of Beirut Medical Center, Beirut, Lebanon.
  • Hourani M; Department of Radiology, American University of Beirut Medical Center, Beirut, Lebanon.
  • Collins M; Section on Skeletal Disorders and Mineral Homeostasis, National Institute of Dental and Craniofacial Research, National Institutes of Health, Bethesda, MD, USA.
  • Ichikawa S; Department of Medicine, Indiana University School of Medicine, Indianapolis, IN, 46202, USA.
  • El Hajj Fuleihan G; Calcium Metabolism and Osteoporosis Program, WHO Collaborating Center for Metabolic Bone Disorders, American University of Beirut Medical Center, Beirut, Lebanon.
Osteoporos Int ; 29(9): 1987-2009, 2018 Sep.
Article em En | MEDLINE | ID: mdl-29923062
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Calcinose / Hiperostose Cortical Congênita / Hiperfosfatemia / Fatores de Crescimento de Fibroblastos / Mutação Tipo de estudo: Diagnostic_studies / Observational_studies Limite: Adolescent / Adult / Female / Humans / Male Idioma: En Revista: Osteoporos Int Ano de publicação: 2018 Tipo de documento: Article
Texto completo
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Calcinose / Hiperostose Cortical Congênita / Hiperfosfatemia / Fatores de Crescimento de Fibroblastos / Mutação Tipo de estudo: Diagnostic_studies / Observational_studies Limite: Adolescent / Adult / Female / Humans / Male Idioma: En Revista: Osteoporos Int Ano de publicação: 2018 Tipo de documento: Article