Massé M, Martinez-Mir A, Lam H, Geraghty M T, Christiano A M
Department of Dermatology, Columbia University, New York, USA.
Clin Exp Dermatol. 2005 Jul;30(4):363-5. doi: 10.1111/j.1365-2230.2005.01762.x.
Identification of mutations in the hairless (HR) gene in patients with atrichia with papular lesions (APL) has proven of critical importance, as it provides a basis for the differentiation between APL and alopecia universalis. The establishment of the diagnostic criteria for APL has triggered the identification of a large number of APL patients among those suspected to suffer from alopecia universalis. This advancement has resulted in the discovery of an increasing number of hairless mutations in both consanguineous and nonconsanguineous APL families. Here, we report the identification of a homozygous mutation, 3434delC, in an APL patient of Arab-Palestinian descent. The proband is a 23-year-old female with generalized scalp and body alopecia. To confirm the diagnosis of APL and to identify the specific mutation, we sequenced the hairless gene. Sequencing of all exons of the hairless gene revealed a homozygous frameshift mutation, 3434delC, in exon 18. Interestingly, the same mutation was previously identified in an Arab-Israeli family. Our data suggest that the 3434delC mutation most likely represents a founder mutation in this geographical region.
丘疹性秃发(APL)患者无毛(HR)基因突变的鉴定已被证明至关重要,因为它为APL和普秃的鉴别诊断提供了依据。APL诊断标准的建立促使在疑似普秃患者中识别出大量APL患者。这一进展导致在近亲通婚和非近亲通婚的APL家族中发现了越来越多的无毛基因突变。在此,我们报告在一名阿拉伯-巴勒斯坦裔APL患者中鉴定出纯合突变3434delC。先证者是一名23岁女性,患有广泛性头皮和全身脱发。为了确诊APL并鉴定特定突变,我们对无毛基因进行了测序。对第18外显子的所有外显子进行测序发现了一个纯合移码突变3434delC。有趣的是,之前在一个阿拉伯-以色列家族中也发现了相同的突变。我们的数据表明,3434delC突变很可能是该地理区域的一个始祖突变。