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Guadalajara camptodactyly syndrome
Authors:J. M. Cantú  ,,H. Rivera,,Z. Nazará  ,,Q. Rojas,,A. Herná  ndez, D. Garcí  a-Cruz,
Affiliation:División de Genética;Subjefatura de Investigatión Científica;Unidad de Investigatión Biomédica y Hospital de Especialidades;Centro Médico de Occidente;Instituto Mexicano del Seguro Social;Guadalajara, Jalisco, Mexico
Abstract:Two sisters, aged 18 and 11 years, were found to have an intrauterine growth retardaion-malformation syndrome which included camptodactyly as a typical sign. The overall analysis of the clinical and radiological findings permitted the individualization of a distinct entity. The family data suggested autosomal recessive inheritance.
Keywords:Camptodactyly    dwarfism    inheritance    autosomal recessive    malformation syndrome.
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