UNI-MB - logo
UMNIK - logo
 
E-viri
Recenzirano Odprti dostop
  • A prenatal case of lissence...
    Balza, Claire; Garofalo, Giulia; Cos, Teresa; Désir, Julie; Kang, Xin; Keymolen, Kathelijn; Soblet, Julie; Van Berkel, Kim; Vilain, Catheline; Ben Abbou, Wafa; Cassart, Marie

    Clinical case reports, December 2021, Letnik: 9, Številka: 12
    Journal Article

    Reelinopathies cause a distinctive lissencephaly type associated with cerebellar hypoplasia. To help further management, we wanted to report here the first prenatal diagnosis due to a homozygous inherited reelinopathy. Reelinopathies cause a distinctive lissencephaly type associated with cerebellar hypoplasia. To help further management, we wanted to report here the first prenatal diagnosis due to a homozygous inherited reelinopathy.