Abstract
Classic galactosemia is an autosomal recessive condition with prevalence of 1:30,000 to 1:50,000. This condition is an example of the genetic metabolic disorder that leads to progressive loss of ovarian function at early age, ultimately causing premature ovarian insufficiency. Here we demonstrate a multidisciplinary approach to ovarian tissue harvesting and cryopreservation from a toddler with galactosemia.
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