Last Updated: 8 August 2024
Last Updated: 8 August 2024
3-M Syndrome
3-M syndrome is a rare genetic disorder characterised by impaired growth and development. Caused by mutations in CUL7, OBSL1, or CCDC8 genes, individuals with 3-M syndrome often experience skeletal abnormalities, short stature and distinct facial features. Intelligence is unaffected by 3-M syndrome, and life expectancy is generally normal. Diagnosis involves clinical evaluation and genetic testing. There is no cure for 3-M syndrome, but supportive treatments can help.
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3-M Syndrome
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