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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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Detalhes bibliográficos
Main Authors: Brancati, Francesco, Sarkozy, Anna, Dallapiccola, Bruno
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2006
Assuntos:
Acesso em linha: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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