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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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Bibliografiset tiedot
Julkaisussa:Iran Red Crescent Med J
Päätekijät: Low, Soo Fin, Abu Bakar, Norzailin, Ngiu, Chai Soon
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Kowsar 2014
Aiheet:
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC4222023/
https://ncbi.nlm.nih.gov/pubmed/25389497
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5812/ircmj.9481
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