posted in Medisage Pediatrics Community

A 12-year-old patient with congenital anomalies or genetic mutation suffered from muscular Dystrophy like syndrome. If any suggestions please add

  • #family health
  • #pediatrics
  • #critical care
  • #academics
  • #general medicine

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Dr. Priya

If clinical phenotype is more in favour of DMD, genetic analysis is preferable and invasive procedures like biopsy can be avoided!!