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Hypoparathyroidism in an Egyptian child with Hutchinson-Gilford progeria syndrome: a case report
INTRODUCTION: Hutchinson-Gilford progeria syndrome is a rare genetic disorder. It is reported to be present in one in eight million and is characterized by severe growth failure, early loss of hair, lipodystrophy, scleroderma, decreased joint mobility, osteolysis, early atherosclerosis and facial fe...
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| Hlavní autoři: | , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
BioMed Central
2012
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| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3269350/ https://ncbi.nlm.nih.gov/pubmed/22251708 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1752-1947-6-17 |
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