Muñoz-Pedroza Liliana A, Arenas-Sordo María L
Servicio de Genética, Asociación Leonesa de Distrofia Muscular S.A. León, Guanajuato, México.
Acta Otorrinolaringol Esp. 2013 Sep-Oct;64(5):359-62. doi: 10.1016/j.otorri.2013.03.007. Epub 2013 Jul 27.
Facio-Auriculo-Vertebral (FAV) spectrum, also known as Goldenhar syndrome or first and second branchial arch syndrome, is a complex of mainly craniofacial and vertebral anomalies. Microtia is a principal malformation in this complex; it can be unilateral or bilateral. We performed an observational, retrospective, transverse descriptive clinical study, reviewing 149 records of patients with a diagnosis of microtia treated in the Genetics Department. There was no significant difference in the sex of the individuals involved. The mean age was 6.97 years, with a range of 1 to 52 years. We founded positive inbreeding in 14 patients and consanguinity in 1 case. There was a family history of microtia in 37 cases. The most frequent malformations, besides microtia, were facial, costo-vertebral, limb, cardiac, genital, eye and other defects. Patients had a high percentage of family history, which could suggest an autosomal dominant inheritance with reduced penetrance.
面-耳-椎(FAV)谱系,也称为Goldenhar综合征或第一和第二鳃弓综合征,是一种主要由颅面和脊柱异常组成的复合体。小耳畸形是该复合体中的主要畸形;可单侧或双侧发生。我们进行了一项观察性、回顾性、横向描述性临床研究,回顾了遗传学部门诊治的149例小耳畸形患者的记录。所涉及个体的性别无显著差异。平均年龄为6.97岁,范围为1至52岁。我们发现14例患者有近亲繁殖,1例有血缘关系。37例有小耳畸形家族史。除小耳畸形外,最常见的畸形是面部、肋椎、肢体、心脏、生殖器、眼睛及其他缺陷。患者有较高比例的家族史,这可能提示常染色体显性遗传且外显率降低。