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与PHACES相关的非随机母源X染色体失活

Non-random maternal X-chromosome inactivation associated with PHACES.

作者信息

Levin J H, Kaler S G

机构信息

Unit on Pediatric Genetics, Laboratory of Clinical Genomics, National Institute of Child Health and Human Development, National Institutes of Health, 10 Center Drive, Bethesda, MD 20892, USA.

出版信息

Clin Genet. 2007 Oct;72(4):345-50. doi: 10.1111/j.1399-0004.2007.00851.x.

Abstract

The acronym PHACES is used to describe the association of posterior fossa malformations, hemangiomas, arterial anomalies (cardiovascular or cerebrovascular), coarctation of the aorta and cardiac defects, eye abnormalities, and sternal or ventral defects. We report a female patient with an uncommon variant of this neurocutaneous disorder who manifested a sternal cleft; supraumbilical raphe; hemangiomas of the face, chest, and extremities; micrognathia and cerebrovascular anomalies. A literature review of PHACES patients with both sternal cleft and supraumbilical raphe showed a marked female predilection. Taken together with cases of sternal cleft, supraumbilical raphe and facial hemangiomas tabulated by Gorlin et al. (1994), 91% (40/44) of patients are female. One affected male died shortly after birth. We hypothesized that the gender bias in PHACES results from mutation in an X-linked dominant gene often lethal in males, and performed X-inactivation analysis of the polymorphic androgen receptor locus in this family. We documented consistently skewed X-inactivation (80%/20% in two independent analyses) in the unaffected mother and consistently random X-inactivation (47:53 and 61:39 in independent analyses) in the proband. These findings are consistent with favorably skewed X-inactivation producing a normal maternal phenotype, a phenomenon documented in X-linked dominant Rett syndrome.

摘要

首字母缩略词PHACES用于描述后颅窝畸形、血管瘤、动脉异常(心血管或脑血管)、主动脉缩窄和心脏缺陷、眼部异常以及胸骨或腹部缺陷之间的关联。我们报告了一名患有这种神经皮肤疾病罕见变异型的女性患者,她表现出胸骨裂、脐上缝、面部、胸部和四肢的血管瘤、小颌畸形和脑血管异常。对同时患有胸骨裂和脐上缝的PHACES患者的文献综述显示,明显女性居多。结合Gorlin等人(1994年)列出的胸骨裂、脐上缝和面部血管瘤病例,91%(40/44)的患者为女性。一名患病男性出生后不久死亡。我们推测PHACES中的性别偏差是由X连锁显性基因的突变导致的,这种突变在男性中往往是致命的,并对该家族中多态性雄激素受体位点进行了X染色体失活分析。我们记录到未受影响的母亲中X染色体失活始终偏向一方(两次独立分析中分别为80%/20%),而先证者中X染色体失活始终是随机的(独立分析中分别为47:53和61:39)

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