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KBG syndrome

KBG syndrome is a rare condition characterised by a typical facial dysmorphism, macrodontia of the upper central incisors, skeletal (mainly costovertebral) anomalies and developmental delay. To date, KBG syndrome has been reported in 45 patients. Clinical features observed in more than half of patie...

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Autores principales: Brancati, Francesco, Sarkozy, Anna, Dallapiccola, Bruno
Formato: Artigo
Lenguaje:Inglês
Publicado: BioMed Central 2006
Materias:
Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC1764006/
https://ncbi.nlm.nih.gov/pubmed/17163996
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1750-1172-1-50
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