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Chinese Journal of Medical Genetics ; (6): 472-475, 2015.
Artigo em Chinês | WPRIM | ID: wpr-288051

RESUMO

<p><b>OBJECTIVE</b>To identify the candidate chromosomal region for congenital preauricular fistula (CPF) through analysis of an affected Chinese family.</p><p><b>METHODS</b>Conventional linkage analysis using short tandem repeats (STR) markers was performed to investigate three chromosomal regions 8q11.1-q13.3, 1q32-q34.3 and 14q31.1-q31.3.</p><p><b>RESULTS</b>None of 16 STRs could attain a LOD score of more than -2.0 (theta=0). Therefore, the three regions were all excluded as the candidate region for the disease.</p><p><b>CONCLUSION</b>CPF features high genetic heterogeneity. The family may have a causative gene elsewhere. Whole-genome-based study is needed to identify its genetic etiology.</p>


Assuntos
Adulto , Feminino , Humanos , Masculino , Povo Asiático , Genética , China , Cromossomos Humanos Par 1 , Genética , Cromossomos Humanos Par 14 , Genética , Cromossomos Humanos Par 8 , Genética , Anormalidades Craniofaciais , Genética , Escore Lod , Repetições de Microssatélites , Linhagem
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