Copyright
©The Author(s) 2020.
World J Clin Cases. Nov 26, 2020; 8(22): 5678-5683
Published online Nov 26, 2020. doi: 10.12998/wjcc.v8.i22.5678
Published online Nov 26, 2020. doi: 10.12998/wjcc.v8.i22.5678
Figure 1 Multiple skin nodules located on the infant’s mother.
Figure 2 Freckle-like depigmentation spots were seen on the chest, abdomen, neck, and left shoulder and armpit.
Figure 3 Large areas of brown pigmentation were noted on the lower limbs, feet, buttocks, and perineum.
Figure 4 Further pedigree validation.
A: Xxx; B: Xxx; C: Xxx.
- Citation: Li MZ, Yuan L, Zhuo ZQ. Gene diagnosis of infantile neurofibromatosis type I: A case report. World J Clin Cases 2020; 8(22): 5678-5683
- URL: https://www.wjgnet.com/2307-8960/full/v8/i22/5678.htm
- DOI: https://dx.doi.org/10.12998/wjcc.v8.i22.5678