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.
Early-onset basal cell carcinoma in a case of Ivemark syndrome
Feliciani, Claudio
2010-01-01
Abstract
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.File in questo prodotto:
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