<i>Hutchinson-Gilford syndrome</i> (progeria)
Progeria is a rare, autosomal dominant, progeroid disorder. In the world literature less than 100 cases have been reported to date. We present this case because of its rarity.
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| Auteurs principaux: | , , , |
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| Format: | Livre |
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Wolters Kluwer Medknow Publications,
2009-01-01T00:00:00Z.
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