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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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| Vydáno v: | Iran Red Crescent Med J |
|---|---|
| Hlavní autoři: | , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Kowsar
2014
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| Témata: | |
| On-line přístup: | 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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