hrp0095p2-173 | Growth and Syndromes | ESPE2022

Case report of Leprechaunism syndrome in an Algerian child

Kherra Sakina , Drali Ouardia , Haddad Karima , Boutaba Mounia , Guichet Anges , Coutant Regis , Zeroual Zoulikha

Introduction: Leprechaunism syndrome is a very rare genetic autosomal recessive disorder (Prevalence 1 in a million births), and is caused by mutations in the insulin receptor gene.Case presentation: We report the case of a 5-month-old Algerian female, born to consanguineous parents. Birth was via caesarean section at 37 weeks gestation due to severe intrauterine growth restriction: birth weight 1800 g (< - 3.66SD), h...