Auriculo-condylar syndrome: Additional patients

Authors

  • Maria Leine Guion-Almeida,

    Corresponding author
    1. Clinical Genetics, Hospital de Reabilitação de Anomalias Craniofaciais, Universidade de São Paulo, Bauru, São Paulo, Brazil
    • Clinical Genetics, HRAC-USP, CEP 17012-900, Bauru, São Paulo, Brazil.
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  • Roseli Maria Zechi-Ceide,

    1. Clinical Genetics, Hospital de Reabilitação de Anomalias Craniofaciais, Universidade de São Paulo, Bauru, São Paulo, Brazil
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  • Siulan Vendramini,

    1. Clinical Genetics, Hospital de Reabilitação de Anomalias Craniofaciais, Universidade de São Paulo, Bauru, São Paulo, Brazil
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  • Nancy Mizue Kokitsu-Nakata

    1. Clinical Genetics, Hospital de Reabilitação de Anomalias Craniofaciais, Universidade de São Paulo, Bauru, São Paulo, Brazil
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Abstract

This report describes several relatives in three generations of one family and another, unrelated boy with auriculo-condylar syndrome, a rare autosomal dominant disorder. Variation in the severity of the abnormalities was observed. We discuss the findings in our patients in relation to those in the literature. © 2002 Wiley-Liss, Inc.

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