摘要
遗传性秃发或少毛症是皮肤科一组比较少见的疾病。根据临床类型不同其具有特征性的临床表现各异。该组疾病的遗传方式可表现为常染色体显性遗传、常染色体隐性遗传和X连锁显性或隐性遗传。在分子遗传学方面,已有多个致病基因位点和/或致病基因被确定,如8p21、6p21、18p11、16q22、18q12、3q26、1p21、Xq13、5q32等致病基因位点和HR、CDH3、CDSN、DSG4、LIPH、ATP7A等基因。
出处
《中国麻风皮肤病杂志》
2008年第9期721-723,共3页
China Journal of Leprosy and Skin Diseases
参考文献20
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同被引文献6
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