Early-onset basal cell carcinoma in a case of Ivemark syndrome

Anna Zampetti, Claudio Feliciani, M Gnarra, D Linder, D Antuzzi, L Cataldi, A Tulli

Risultato della ricerca: Contributo in rivistaArticolo in rivista

1 Citazioni (Scopus)


First described by the Swedish paediatrician, Björn Ivemark, (1925-2005), IS is a rare congenital heterotaxic disorder with lateralization anomalies [1]. It accounts for 1- 3% of all congenital heart defects, with an incidence of 1 in 10-20,000 live births. To date, about 200 cases have been reported in the literature, mostly sporadic, but familial occurrence has also been described, suggesting autosomal recessive inheritance, with a male preponderance.
Lingua originaleEnglish
pagine (da-a)845-846
Numero di pagine2
RivistaEuropean Journal of Dermatology
Stato di pubblicazionePubblicato - 2010
Pubblicato esternamenteYes


  • Abnormalities, Multiple
  • Carcinoma, Basal Cell
  • Female
  • Heart Defects, Congenital
  • Heterotaxy Syndrome
  • Humans
  • Shoulder
  • Skin Neoplasms
  • Splenic Diseases
  • Young Adult

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