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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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| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
BioMed Central
2012
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| Online Zugang: | 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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