<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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Bibliografiske detaljer
Main Authors: Surjushe Amar (Author), Thakre Minal (Author), Vasani Resham (Author), Saple Dattatray (Author)
Format: Bog
Udgivet: Wolters Kluwer Medknow Publications, 2009-01-01T00:00:00Z.
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3rd Floor Main Library

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Klassifikationsnummer: A1234.567
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