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A report of two children with Gorham-Stout disease
BACKGROUND: Gorham-Stout disease is a rare condition characterized by unifocal and massive type IV osteolysis (variant of idiopathic nonhereditary osteolytic disease) with a slow progression, which is self-limiting for some years. It is characterized by recurrent vascular tumors with disruption of t...
Uloženo v:
| Vydáno v: | BMC Pediatr |
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| Hlavní autoři: | , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
BioMed Central
2019
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6591827/ https://ncbi.nlm.nih.gov/pubmed/31234820 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12887-019-1561-0 |
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