Of particular interest in this case, the patient had a significant amount of polyhydramnios, which could have facilitated uterine torsion through increasing uterine size and enhancing rotational instability. An additional noteworthy aspect of this case is the postnatal diagnosis of X-linked myotubular myopathy (XLMTM) in the neonate, with subsequent genetic testing confirming the mother's carrier status for the MTM1 gene mutation. The gene discussed is MTM1; the disease is X-linked myotubular myopathy.