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Hutchinson – Gilford progeria syndrome: A rare case report
Hutchinson – Gilford Progeria Syndrome is a rare genetic disorder characterized by premature aging involving the skin, bones, heart, and blood vessels. We report a three-year-old boy with clinical manifestations characteristic of this syndrome. He had a characteristic “plucked-bird” appearance, prom...
Wedi'i Gadw mewn:
| Cyhoeddwyd yn: | Indian Dermatol Online J |
|---|---|
| Prif Awduron: | , , |
| Fformat: | Artigo |
| Iaith: | Inglês |
| Cyhoeddwyd: |
Medknow Publications & Media Pvt Ltd
2014
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| Pynciau: | |
| Mynediad Ar-lein: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4228646/ https://ncbi.nlm.nih.gov/pubmed/25396134 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/2229-5178.142507 |
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