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Meckel-Gruber syndrome

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Description

Meckel syndrome (MKS) is a rare, lethal, genetic, multiple congenital anomaly disorder characterized by the triad of brain malformation (mainly occipital encephalocele), large polycystic kidneys, and polydactyly, as well as associated abnormalities that may include cleft lip/palate, cardiac and genital anomalies, central nervous system (CNS) malformations, liver fibrosis, and bone dysplasia.

ORDO

  • Mode of Inheritance

    VARIANTS

    1,689

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    Genes

    External Links

    • OMIM
    • Orphanet

      564

    • HPO
    • Medgen

      C0265215

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