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Congenital Milroy Oedema: a case report of a family

La Pediatria medica e chirurgica, 2012-03, Vol.34 (2), p.100-103 [Peer Reviewed Journal]

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Title:
Congenital Milroy Oedema: a case report of a family
Author: Raffa, V ; Campra, D ; Guarino, R ; Angellotti, P ; Ballardini, G ; Boscardini, L ; Guala, A
Subjects: Edema congenito ; gene VEGFR3 ; Humans ; Infant ; Lymphedema - congenital ; Lymphedema - genetics ; Male ; sindrome di Milroy
Is Part Of: La Pediatria medica e chirurgica, 2012-03, Vol.34 (2), p.100-103
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.
Publisher: Italy: PAGEPress Publications
Language: Italian;English
Identifier: ISSN: 0391-5387
EISSN: 2420-7748
DOI: 10.4081/pmc.2012.68
PMID: 22730636
Source: MEDLINE
DOAJ Directory of Open Access Journals

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