Copyright
©The Author(s) 2025.
World J Clin Pediatr. Dec 9, 2025; 14(4): 109874
Published online Dec 9, 2025. doi: 10.5409/wjcp.v14.i4.109874
Published online Dec 9, 2025. doi: 10.5409/wjcp.v14.i4.109874
Figure 1
The shows clinical features of microcephaly, short stature, and abnormal hand movements in a patient with Rett syndrome.
Figure 2 The shows an abnormal female karyotype 46,XX, del(15)(q22qter).
Orange arrow shows the terminal deletion in chromosome 15.
Figure 3
The shows normal findings of the magnetic resonance imaging of the brain.
- Citation: Fadl-Elmula I, Abdel-Raheem SY, Khalid R. Atypical case of Rett syndrome with concurrent MECP2 gene mutation and del(15)(q22qter) karyotype: A case report and review of literature. World J Clin Pediatr 2025; 14(4): 109874
- URL: https://www.wjgnet.com/2219-2808/full/v14/i4/109874.htm
- DOI: https://dx.doi.org/10.5409/wjcp.v14.i4.109874
