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Disruption of the PTHLH regulatory landscape results in features consistent with hyperparathyroid disease.
Deshwar, Ashish R; Spielmann, Malte; Vi, Lisa; Mendoza-Londono, Roberto; Dupuis, Lucie; Stimec, Jennifer; Howard, Andrew; Harrington, Jennifer; Kannu, Peter.
Afiliação
  • Deshwar AR; Division of Clinical and Metabolic Genetics and University of Toronto, Department of Paediatrics, The Hospital for Sick Children, Toronto, Ontario, Canada.
  • Spielmann M; Medical Genetics Residency Training Program, University of Toronto, Toronto, Ontario, Canada.
  • Vi L; Department of Genome Sciences, University of Washington, Seattle, Western Australia.
  • Mendoza-Londono R; Program in Developmental and Stem Cell Biology, University of Toronto, Canada.
  • Dupuis L; Division of Clinical and Metabolic Genetics and University of Toronto, Department of Paediatrics, The Hospital for Sick Children, Toronto, Ontario, Canada.
  • Stimec J; Division of Clinical and Metabolic Genetics and University of Toronto, Department of Paediatrics, The Hospital for Sick Children, Toronto, Ontario, Canada.
  • Howard A; Department of Diagnostic Imaging, The Hospital for Sick Children, Toronto, Ontario, Canada.
  • Harrington J; Division of Orthopaedics, University of Toronto and The Hospital for Sick Children, Toronto, Ontario, Canada.
  • Kannu P; Division of Endocrinology, Department of Paediatrics, Hospital for Sick Children, University of Toronto, Toronto, Ontario, Canada.
Am J Med Genet A ; 179(4): 663-667, 2019 04.
Article em En | MEDLINE | ID: mdl-30803154
Parathyroid hormone like hormone (PTHLH) signaling is essential for the proper formation of bone and its elevation or disruption has been directly implicated in several different skeletal dysplasias. We report a patient with a 2.802 Mb deletion upstream of the PTHLH coding sequence who presents with multiple fractures, metaphyseal changes, and overall features consistent with hyperparathyroid like disease. Analysis of the deleted region revealed the loss of putative regulatory regions adjacent to PTHLH and the possible gain of a limb enhancer. Furthermore, PTHLH expression appeared to be mis-regulated in fibroblasts derived from the patient. Altogether, we find that the disruption of the regulatory landscape of PTHLH likely results in its inappropriate expression and this novel clinical presentation.
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Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Sequências Reguladoras de Ácido Nucleico / Proteína Relacionada ao Hormônio Paratireóideo / Hiperparatireoidismo / Mutação Tipo de estudo: Prognostic_studies Limite: Child / Humans / Male Idioma: En Revista: Am J Med Genet A Assunto da revista: GENETICA MEDICA Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Canadá

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Sequências Reguladoras de Ácido Nucleico / Proteína Relacionada ao Hormônio Paratireóideo / Hiperparatireoidismo / Mutação Tipo de estudo: Prognostic_studies Limite: Child / Humans / Male Idioma: En Revista: Am J Med Genet A Assunto da revista: GENETICA MEDICA Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Canadá