Disruption of the PTHLH regulatory landscape results in features consistent with hyperparathyroid disease.
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.
Palavras-chave
Texto completo:
1
Bases de dados:
MEDLINE
Assunto principal:
Sequências Reguladoras de Ácido Nucleico
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Proteína Relacionada ao Hormônio Paratireóideo
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Hiperparatireoidismo
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Mutação
Tipo de estudo:
Prognostic_studies
Limite:
Child
/
Humans
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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