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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


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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.

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