Linfedema primario (Sindrome di Nonne-Milroy): Descrizione di quattro casi

Translated title of the contribution: Congenital lymphedema syndrome (Nonne-Milroy disease): Report of four cases

L. Bruni, A. Torre, R. Capolino, M. C. Tozzi, M. Bavastrelli, M. Midulla

Research output: Contribution to journalArticlepeer-review

Abstract

Nonne-Milroy syndrome is a rare genetic disorder mainly with autosomic dominant trasmission, characterized by primary lymphedema generally of the leg and the foot at one or both sides. Lymphedema is apparent from birth and sometimes affects also the hands and rarely male genitalia, and persists for life. Four cases of Nonne-Milroy syndrome, with different clinical pictures, observed in the last fifteen years, in Pediatric Department University «La Sapienza» of Rome, are reported.

Translated title of the contributionCongenital lymphedema syndrome (Nonne-Milroy disease): Report of four cases
Original languageItalian
Pages (from-to)494-498
Number of pages5
JournalRivista Italiana di Pediatria
Volume24
Issue number3 SUPPL.
Publication statusPublished - 1998

ASJC Scopus subject areas

  • Pediatrics, Perinatology, and Child Health

Fingerprint

Dive into the research topics of 'Congenital lymphedema syndrome (Nonne-Milroy disease): Report of four cases'. Together they form a unique fingerprint.

Cite this