New Phenotypic Feature in a Patient With a Rare Triplication of the 22q11.2 Region Presenting With Peters Anomaly, Congenital Heart Disease, and Global Developmental Delay: A Case Report and Literature Review

Isra Idris; Abinash Pandey; Abdalaziz M. Awadelkarim; Eltaib A. Saad; Marsha Medows; Isra Idris; Abinash Pandey; Abdalaziz M. Awadelkarim; ELTAIB SAAD; Marsha Medows

doi:10.7759/cureus.26071

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