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    Larsen Syndrome: A Case Report with a Brief Review of the Literature
    (Duzce Univ, 2013) Sarman, Hakan; Memisoglu, Kaya; Baran, Tuncay
    Larsen syndrome is a rare genetic disorder, with an incidence of 1/100,000. Joint hypermobility, congenital joint dislocations, spinal deformity and distinctive facial features are characteristic findings in the newborns. Congenital orthopedics pathology is rare with this syndrome. Herein we present a case with Larsen syndrome and discuss it with a brief review of the literature.