The KBG syndrome, characteristic dental findings: a case report
2001; Wiley; Volume: 11; Issue: 2 Linguagem: Inglês
10.1046/j.1365-263x.2001.00231.x
ISSN1365-263X
AutoresPaul Dowling, Padhraig S. Fleming, Robert J. Gorlin, Marissa King, N. C. Nevin, Meriel McEntagart,
Tópico(s)Hedgehog Signaling Pathway Studies
ResumoShort stature and developmental delay may be observed in many genetic conditions and well‐defined syndromes. A 7‐year‐old girl presented with the non‐specific findings of subtle dysmorphism, short stature and developmental delay. Although a genetic syndrome was suspected, a definitive diagnosis was not made until the dental findings of KBG syndrome were recognised, namely grossly enlarged maxillary permanent central incisors and hypodontia.
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