Copyright
©The Author(s) 2021.
World J Clin Cases. Nov 26, 2021; 9(33): 10257-10264
Published online Nov 26, 2021. doi: 10.12998/wjcc.v9.i33.10257
Published online Nov 26, 2021. doi: 10.12998/wjcc.v9.i33.10257
Figure 1 Facial features of the patient.
At age 3 mo, he had a long palpebral fissure (A), arched and broad eyebrows with the lateral third displaying sparseness (B), long eyelashes (A), but short columella with depressed nasal tip (C), wide nasal bridge, and high-arched palate as well as a high forehead and hairline (D).
- Citation: Guo HX, Li BW, Hu M, Si SY, Feng K. Novel KDM6A mutation in a Chinese infant with Kabuki syndrome: A case report. World J Clin Cases 2021; 9(33): 10257-10264
- URL: https://www.wjgnet.com/2307-8960/full/v9/i33/10257.htm
- DOI: https://dx.doi.org/10.12998/wjcc.v9.i33.10257