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22 August 2022
: Case report 
Rare disease, Congenital defects / diseases
Moulay Omar Moustaine1ABCDEF*, Mohammed Frarchi1AEF, Majd Haloui1ABE, Fatima Zahra Chabbab2AEDOI: 10.12659/AJCR.935544
Am J Case Rep 2022; 23:e935544
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