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    A Clinical Case of CNOT3 Syndrome in a 10-Year-Old Girl

    E. E. Baranova, I. M. Osmanov, I.D. Maykova … Zakharova In
    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.
    Automatically generated from the study's abstract, not written by a person, and not a review of the full paper. Not medical advice or a treatment recommendation. Read the original study, and consult a qualified healthcare professional before changing treatment. Full disclaimer
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