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Anil Soni

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Open access Sep 2026

Syndromic Congenital Heart Disease in a Child with 6q24.3-q25.1 Microdeletion: A Case Report with Genotype–Phenotype Correlation

Chromosome 6q24.3-q25.1 microdeletion syndrome is a rare contiguous gene deletion disorder associated with multilevel congenital heart defects, growth abnormalities, and dysmorphic features. We report the case of an 8-month-old female child who presented with fever, cough, and respiratory distress. She had a history of...

Kritika Goel, Sarthak Kaushik, Renu Sharma et al. · 0 citations

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