A Clinical Case of CNOT3 Syndrome in a 10-Year-Old Girl
December 2025
in “
Meditsinskiy sovet = Medical Council
”
Studysummary This case study highlights the importance of an integrated diagnostic and treatment approach for children with rare genetic disorders, as demonstrated in a 10-year-old girl with CNOT3 syndrome, characterized by symptoms like mental retardation, gastrointestinal issues, and unique facial features.
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