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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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| Fformat: | Artigo |
| Iaith: | Inglês |
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BioMed Central
2008
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| Mynediad Ar-lein: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2565666/ https://ncbi.nlm.nih.gov/pubmed/18822138 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1757-1626-1-186 |
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