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The KBG syndrome: Case report

INTRODUCTION: The KBG syndrome is a rare autosomal dominant condition, first described by Hermann et al. in 1975. Fundamental findings are: mild development delay, short stature, craniofacial dysmorphism and skeletal anomalies. CASE PRESENTATION: A 32 years old woman, Caucasian race, weight 57 Kg, a...

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Detalles Bibliográficos
Autores principales: Morghen, Ilaria, Ferri, Enrico
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2565666/
https://www.ncbi.nlm.nih.gov/pubmed/18822138
http://dx.doi.org/10.1186/1757-1626-1-186