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.
| Original language | Italian |
|---|---|
| Pages (from-to) | 494-498 |
| Number of pages | 5 |
| Journal | Rivista Italiana di Pediatria |
| Volume | 24 |
| Issue number | 3 SUPPL. |
| Publication status | Published - 1998 |
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ASJC Scopus subject areas
- Pediatrics, Perinatology, and Child Health
Cite this
Linfedema primario (Sindrome di Nonne-Milroy) : Descrizione di quattro casi. / Bruni, L.; Torre, A.; Capolino, R.; Tozzi, M. C.; Bavastrelli, M.; Midulla, M.
In: Rivista Italiana di Pediatria, Vol. 24, No. 3 SUPPL., 1998, p. 494-498.Research output: Contribution to journal › Article
}
TY - JOUR
T1 - Linfedema primario (Sindrome di Nonne-Milroy)
T2 - Descrizione di quattro casi
AU - Bruni, L.
AU - Torre, A.
AU - Capolino, R.
AU - Tozzi, M. C.
AU - Bavastrelli, M.
AU - Midulla, M.
PY - 1998
Y1 - 1998
N2 - 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.
AB - 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.
KW - Congenital lymphedema
KW - Nonne-Milroy disease
UR - http://www.scopus.com/inward/record.url?scp=0039076575&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0039076575&partnerID=8YFLogxK
M3 - Articolo
AN - SCOPUS:0039076575
VL - 24
SP - 494
EP - 498
JO - Rivista Italiana di Pediatria
JF - Rivista Italiana di Pediatria
SN - 0392-5161
IS - 3 SUPPL.
ER -