Literature DB >> 22730636

[Congenital Milroy Oedema: a case report of a family].

V Raffa, D Campra, R Guarino, P Angellotti, G Ballardini, L Boscardini, A Guala.   

Abstract

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.

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Year:  2012        PMID: 22730636     DOI: 10.4081/pmc.2012.68

Source DB:  PubMed          Journal:  Pediatr Med Chir        ISSN: 0391-5387


  1 in total

1.  Four generations of rare familial lymphedema (Milroy disease).

Authors:  Sankalp Gokhale; Sanjay Gokhale
Journal:  Med Princ Pract       Date:  2013-06-04       Impact factor: 1.927

  1 in total

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