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Radiol Case Rep ; 9(2): 911, 2014.
Artículo en Inglés | MEDLINE | ID: mdl-27186241

RESUMEN

The extremely rare Proteus Syndrome is a hamartomatous congenital syndrome with substantial variability between clinical patient presentations. The diagnostic criteria consist of a multitude of clinical findings including hemihypertrophy, macrodactyly, epidermal nevi, subcutaneous hamartomatous tumors, and bony abnormalities. These clinical findings correlate with striking radiographic findings.

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