Congenital Milroy Oedema: a case report of a family
Abstract
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.Downloads
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Published
2012-04-30
Keywords:
Edema congenito, sindrome di Milroy, gene VEGFR3
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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
Copyright (c) 2012 V. Raffa, D. Campra, R. Guarino, P. Angellotti, G. Ballardini, L. Boscardini, A. Guala

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