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Pierre Robinov syndróm

  1. Subject h.Pierre Robinov syndróm
    Subject h.Pierre Robin Syndrome
    Entry termsPierre Robinova sekvencia
    micrognatia-glossoptosis congenitalis
    Robinova sekvencia
    Robinov syndróm
    glosoptóza, mikrognatia a rázštep podnebia
    Scope note in EnglishCongenital malformation characterized by MICROGNATHIA or RETROGNATHIA; GLOSSOPTOSIS and CLEFT PALATE. The mandibular abnormalities often result in difficulties in sucking and swallowing. The syndrome may be isolated or associated with other syndromes (e.g., ANDERSEN SYNDROME; CAMPOMELIC DYSPLASIA). Developmental mis-expression of SOX9 TRANSCRIPTION FACTOR gene on chromosome 17q and its surrounding region is associated with the syndrome.
    See also reference (FX) in Slovak Andersenov syndróm
    dysplázia kampomelická
    faktor transkripčný SOX9
    See also reference (FX) in English Andersen Syndrome
    Campomelic Dysplasia
    SOX9 Transcription Factor
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    (3) - MeSH descriptor
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Number of the records: 1  

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