File:Kbg2.jpg
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| Description | Frontal (a) and lateral (b) view of a KBG syndrome patient with typical facial dysmorphisms including low frontal hairline, wide eyebrows with mild synophrys, hypertelorism, prominent and high nasal bridge, anteverted nostrils, long philtrum, thin upper lip and prominent anteverted ears |
| Date | |
| Source | Brancati, F, Sarkozy, A, Dallapiccola, B. KBG syndrome. Orphanet Journal of Rare Diseases. 1, 50. 2006. PMID 17163996. |
| Author | see above |
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| Date/Time | Thumbnail | Dimensions | User | Comment | |
|---|---|---|---|---|---|
| current | 16:41, 8 August 2007 | | 1,200 × 626 (170 KB) | Filip em | {{Information |Description=Frontal (a) and lateral (b) view of a KBG syndrome patient with typical facial dysmorphisms including low frontal hairline, wide eyebrows with mild synophrys, hypertelorism, prominent and high nasal bridge, anteverted nostrils, |
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