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Intermediate type of Juvenile Paget's disease: A rare case in Indian population
Author(s) -
Sachin Kumar,
Bhavana S Bagalad,
Ch Balakrishna Manohar,
Puneeth Horatti Kuberappa
Publication year - 2017
Publication title -
contemporary clinical dentistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.289
H-Index - 21
eISSN - 0976-237X
pISSN - 0976-2361
DOI - 10.4103/ccd.ccd_1097_16
Subject(s) - medicine , disease , juvenile , skeletal disorder , genetic disorder , population , pediatrics , rare disease , pathology , environmental health , osteoporosis , genetics , biology
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.

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