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An unusual case of KBG syndrome with unique oral findings
KBG syndrome is a condition characterised by macrodontia, neurological disturbance, short stature, a distinct cranio-facial appearance, and skeletal anomalies. The authors describe what appears to be the first case of KBG syndrome reported from the Indian subcontinent. Meticulous evaluation of the d...
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| Pubblicato in: | BMJ Case Rep |
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| Autori principali: | , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
BMJ Publishing Group
2015
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4513503/ https://ncbi.nlm.nih.gov/pubmed/26187867 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/bcr-2015-210352 |
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