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Gazzetta Medica Italiana Archivio per le Scienze Mediche 2006 August;165(4):159-65
Copyright © 2006 EDIZIONI MINERVA MEDICA
language: English, Italian
Leopard Syndrome: clinical presentation, molecular analysis and genotypo-phenotypo correlation
Cesare G., Limongelli G., Pacileo G., Miele T., Ancona R., Verrengia M., Russo G., Calabrò R.
Chair of Cardiology, Department of Pediatric Cardiology “A.O. Monaldi”, Second University of Naples, Naples, Italy
Leopard Syndrome is a extremely rare disease, autosomal dominant, characterized from a series of systemich anomalies (cutaneous, facial, genital etc), between which the cardiovascular anomalies they assume a relief rolesure,
“Leopard” is an acronym that was introduced from Gorlin.