Congenital Milroy Oedema: a case report of a family

Submitted: 18 November 2014
Accepted: 18 November 2014
Published: 30 April 2012
Abstract Views: 1123
PDF: 4655
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Authors

The authors describe the case of a newborn and their family with Nonne-Milroy disease (hereditary lymphedema type I), a genetic disease that is usually characterized by lymphedema, that most often affects the lower extremities or less frequently the back of the hands. We discuss etiology, inheritance pattern, differential diagnosis and follow-up.

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How to Cite

Raffa, V., Campra, D., Guarino, R., Angellotti, P., Ballardini, G., Boscardini, L., & Guala, A. (2012). Congenital Milroy Oedema: a case report of a family. La Pediatria Medica E Chirurgica, 34(2). https://doi.org/10.4081/pmc.2012.68

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