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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Formaat: | Artikel |
Taal: | English |
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PAGEPress Publications
2012-04-01
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Reeks: | La Pediatria Medica e Chirurgica |
Onderwerpen: | |
Online toegang: | http://www.pediatrmedchir.org/index.php/pmc/article/view/68 |
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author | V. Raffa D. Campra R. Guarino P. Angellotti G. Ballardini L. Boscardini A. Guala |
author_facet | V. Raffa D. Campra R. Guarino P. Angellotti G. Ballardini L. Boscardini A. Guala |
author_sort | V. Raffa |
collection | DOAJ |
description | 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. |
first_indexed | 2024-12-10T11:33:06Z |
format | Article |
id | doaj.art-ee17ca2f9ff24f76b800f242cb8e47e7 |
institution | Directory Open Access Journal |
issn | 0391-5387 2420-7748 |
language | English |
last_indexed | 2024-12-10T11:33:06Z |
publishDate | 2012-04-01 |
publisher | PAGEPress Publications |
record_format | Article |
series | La Pediatria Medica e Chirurgica |
spelling | doaj.art-ee17ca2f9ff24f76b800f242cb8e47e72022-12-22T01:50:32ZengPAGEPress PublicationsLa Pediatria Medica e Chirurgica0391-53872420-77482012-04-0134210.4081/pmc.2012.6868Congenital Milroy Oedema: a case report of a familyV. Raffa0D. Campra1R. Guarino2P. Angellotti3G. Ballardini4L. Boscardini5A. Guala6SOC Pediatria, Ospedale Castelli, Verbania ASL VCO Regione PiemontePediatra di Libera Scelta, ASL VC Regione PiemonteSOC Pediatria, Ospedale di Taormina, Regione SiciliaSOC Pediatria, Ospedale Castelli, Verbania ASL VCO Regione PiemonteSOC Pediatria, Ospedale Castelli, Verbania ASL VCO Regione PiemonteSOC Pediatria, Ospedale Castelli, Verbania ASL VCO Regione PiemonteSOC Pediatria, Ospedale Castelli, Verbania ASL VCO Regione PiemonteThe 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.http://www.pediatrmedchir.org/index.php/pmc/article/view/68Edema congenitosindrome di Milroygene VEGFR3 |
spellingShingle | V. Raffa D. Campra R. Guarino P. Angellotti G. Ballardini L. Boscardini A. Guala Congenital Milroy Oedema: a case report of a family La Pediatria Medica e Chirurgica Edema congenito sindrome di Milroy gene VEGFR3 |
title | Congenital Milroy Oedema: a case report of a family |
title_full | Congenital Milroy Oedema: a case report of a family |
title_fullStr | Congenital Milroy Oedema: a case report of a family |
title_full_unstemmed | Congenital Milroy Oedema: a case report of a family |
title_short | Congenital Milroy Oedema: a case report of a family |
title_sort | congenital milroy oedema a case report of a family |
topic | Edema congenito sindrome di Milroy gene VEGFR3 |
url | http://www.pediatrmedchir.org/index.php/pmc/article/view/68 |
work_keys_str_mv | AT vraffa congenitalmilroyoedemaacasereportofafamily AT dcampra congenitalmilroyoedemaacasereportofafamily AT rguarino congenitalmilroyoedemaacasereportofafamily AT pangellotti congenitalmilroyoedemaacasereportofafamily AT gballardini congenitalmilroyoedemaacasereportofafamily AT lboscardini congenitalmilroyoedemaacasereportofafamily AT aguala congenitalmilroyoedemaacasereportofafamily |