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vol.101 número2REPORTE DE CASO: PURPURA DISEMINADA COMO PRIMERA MANIFESTACIÓN DE SÍNDROME DE DRESSQUERATOSIS SEBORREICA: VARIANTE CLONAL. REPORTE DE UN CASO. índice de autoresíndice de materiabúsqueda de artículos
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Revista argentina de dermatología

versión On-line ISSN 1851-300X

Resumen

MARES-CHIYON, A; DAVALOS-SORIA, D  y  ALVAREZ-VARGAS, M. CLOVES syndrome: case report and review of differential diagnoses. Rev. argent. dermatol. [online]. 2020, vol.101, n.2, pp.41-50. ISSN 1851-300X.

We present the case of a 27-years-old patient with a newly diagnosis of CLOVES syndrome (Congenital, Lipomatous, Overgrowth, Vascular malformations, Epidermal nevi and Spinal/Skeletal anomalies and/or Scoliosis Syndrome). She has previously been diagnosed of Klippel-Trenaunay-Weber (at birth) and Proteus Syndrome (at 7 years). She presents dermatological alterations, syndactyly and overgrowth. CLOVES syndrome is a rare disease and often the clinic-based diagnostic is difficult due to overlapping signs and symptoms with other illnesses that also involve overgrowth.

Palabras clave : CLOVES; Proteus; Klippel-Trenaunay-Weber; Overgrowth syndrome.

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