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Leopard syndrome

LEOPARD syndrome (LS, OMIM 151100) is a rare multiple congenital anomalies condition, mainly characterized by skin, facial and cardiac anomalies. LEOPARD is an acronym for the major features of this disorder, including multiple Lentigines, ECG conduction abnormalities, Ocular hypertelorism, Pulmonic...

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Detalles Bibliográficos
Autores principales: Sarkozy, Anna, Digilio, Maria Cristina, Dallapiccola, Bruno
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2467408/
https://www.ncbi.nlm.nih.gov/pubmed/18505544
http://dx.doi.org/10.1186/1750-1172-3-13