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Intermediate Type of Juvenile Paget's Disease: A Rare Case in Indian Population

Juvenile Paget's disease (JPD), a rare genetic skeletal disorder characterized by accelerated bone turnover with elevated levels of serum alkaline phosphatase, presents in early childhood. We report a female patient with typical features of JPD with dental finding who remained undiagnosed until...

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Detalles Bibliográficos
Autores principales: Kumar, S. Ravi Raja, Bagalad, Bhavana S., Manohar, Ch. Balakrishna, Kuberappa, Puneeth H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5426156/
https://www.ncbi.nlm.nih.gov/pubmed/28566875
http://dx.doi.org/10.4103/ccd.ccd_1097_16
Descripción
Sumario:Juvenile Paget's disease (JPD), a rare genetic skeletal disorder characterized by accelerated bone turnover with elevated levels of serum alkaline phosphatase, presents in early childhood. We report a female patient with typical features of JPD with dental finding who remained undiagnosed until 18 years of age. Scarcity of this disease in the Indian literature and need for timely diagnosis to avert progression of disease thus incited us to report this case.