Copyright
©The Author(s) 2023.
World J Clin Cases. Mar 26, 2023; 11(9): 2036-2042
Published online Mar 26, 2023. doi: 10.12998/wjcc.v11.i9.2036
Published online Mar 26, 2023. doi: 10.12998/wjcc.v11.i9.2036
Figure 1 Pedigree map of the family.
Figure 2 Distinctive facial features.
A: Round face, stubby nose, forward-leaned nostrils and thick lips; B: Long eyelashes.
Figure 3 Representative radiographic images.
A: Delayed bone age; B: Beak-like femur head; C: Lumbar lordosis.
Figure 4 Age and height curve.
rhGH: Recombinant human growth hormone; SD: Standard deviation.
- Citation: Shen R, Feng JH, Yang SP. Acromicric dysplasia caused by a mutation of fibrillin 1 in a family: A case report. World J Clin Cases 2023; 11(9): 2036-2042
- URL: https://www.wjgnet.com/2307-8960/full/v11/i9/2036.htm
- DOI: https://dx.doi.org/10.12998/wjcc.v11.i9.2036