Congenital Milroy Oedema: a case report of a family
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, inheritanc...
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PAGEPress Publications,
2012-04-01T00:00:00Z.
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| 001 | doaj_ee17ca2f9ff24f76b800f242cb8e47e7 | ||
| 042 | |a dc | ||
| 100 | 1 | 0 | |a V. Raffa |e author |
| 700 | 1 | 0 | |a D. Campra |e author |
| 700 | 1 | 0 | |a R. Guarino |e author |
| 700 | 1 | 0 | |a P. Angellotti |e author |
| 700 | 1 | 0 | |a G. Ballardini |e author |
| 700 | 1 | 0 | |a L. Boscardini |e author |
| 700 | 1 | 0 | |a A. Guala |e author |
| 245 | 0 | 0 | |a Congenital Milroy Oedema: a case report of a family |
| 260 | |b PAGEPress Publications, |c 2012-04-01T00:00:00Z. | ||
| 500 | |a 10.4081/pmc.2012.68 | ||
| 500 | |a 0391-5387 | ||
| 500 | |a 2420-7748 | ||
| 520 | |a 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. | ||
| 546 | |a EN | ||
| 546 | |a IT | ||
| 690 | |a Edema congenito | ||
| 690 | |a sindrome di Milroy | ||
| 690 | |a gene VEGFR3 | ||
| 690 | |a Pediatrics | ||
| 690 | |a RJ1-570 | ||
| 690 | |a Surgery | ||
| 690 | |a RD1-811 | ||
| 655 | 7 | |a article |2 local | |
| 786 | 0 | |n La Pediatria Medica e Chirurgica, Vol 34, Iss 2 (2012) | |
| 787 | 0 | |n http://www.pediatrmedchir.org/index.php/pmc/article/view/68 | |
| 787 | 0 | |n https://doaj.org/toc/0391-5387 | |
| 787 | 0 | |n https://doaj.org/toc/2420-7748 | |
| 856 | 4 | 1 | |u https://doaj.org/article/ee17ca2f9ff24f76b800f242cb8e47e7 |z Connect to this object online. |