RESUMEN

The authors report on a case of a 7-days old girls, with Nonne-Milroy syndrome (type I hereditary lynphedema). The clinical picture of this disease is severe but the outcome is usually good. Its etiology, differential diagnosis, therapy and follow-up are discussed.

Asunto(s)

Linfedema/congénito , Femenino , Humanos , Recién Nacido , Linfedema/clasificación , Linfedema/diagnóstico , Síndrome