Camurati-Engelmann Disease Association With Hypogonadism and Primary Hypothyroidism

INTRODUCTION: Camurati-Engelmann disease (CED) is a rare autosomal dominant disease with various phenotypic expressions. The symptoms usually develop during childhood. The hallmark of the disease is bilateral symmetric diaphyseal hyperostosis of the long bones with progressive involvement of the met...

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Detalles Bibliográficos
Autores principales: Low, Soo Fin, Abu Bakar, Norzailin, Ngiu, Chai Soon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Kowsar 2014
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4222023/
https://www.ncbi.nlm.nih.gov/pubmed/25389497
http://dx.doi.org/10.5812/ircmj.9481

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4222023/
https://www.ncbi.nlm.nih.gov/pubmed/25389497
http://dx.doi.org/10.5812/ircmj.9481

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