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Spondylo-camptodactyly syndrome: a distinct autosomal dominant entity?
L A Lizcano-Gil1, D García-Cruz, J Sánchez-Corona
1Maestría en Genética Humana, Universidad de Guadalajara, Jalisco, México.
Clinical Genetics
|October 1, 1995
Abstract:
We present a family in which five members over three generations have a syndrome characterized by camptodactyly, flattened bodies of cervical vertebrae, and a variable degree of thoracic scoliosis. After excluding other camptodactyly syndromes, it was concluded that this association of anomalies probably represents a new autosomal dominant syndrome.