Baumeister F A, Egger J, Schildhauer M T, Stengel-Rutkowski S
Dr. v. Haunersches Kinderspital, Universität München, Germany.
Clin Genet. 1993 Sep;44(3):121-8. doi: 10.1111/j.1399-0004.1993.tb03862.x.
Congenital hypertrichosis universalis is a rare autosomal dominant disease. We report the further development of a Greek girl, now aged 3 years, the first case associated with a balanced structural chromosomal aberration. She was described as a neonate by Sigalas et al. (1990). Her persistent generalized hypertrichosis is most excessive on the face, ears and shoulders. Her fine silky hair is of the vellus, not the lanugo type. The syndrome features are characterized, referring to nine further published case reports. It is distinguished from other types of congenital hypertrichoses, which have been described in the literature under different synonyms. To avoid confusion in the terminology, we propose to name this type of hypertrichosis Ambras syndrome in reference to the first documented family with congenital hypertrichosis universalis in the 16th century.
先天性全身多毛症是一种罕见的常染色体显性疾病。我们报告了一名现年3岁的希腊女孩的进一步病情发展,她是首例与平衡性结构染色体畸变相关的病例。1990年,西加拉等人将她作为新生儿进行了描述。她持续性的全身多毛症在面部、耳朵和肩部最为严重。她的细软丝发属于毳毛,而非胎毛类型。参考另外九篇已发表的病例报告,对该综合征的特征进行了描述。它与文献中以不同同义词描述的其他类型先天性多毛症有所区别。为避免术语混淆,我们建议将这种多毛症类型命名为安布拉斯综合征,以纪念16世纪首个有记录的先天性全身多毛症家族。