Beillard Charlotte, Guillet Gérard, Vabres Pierre, Dagregorio Guy, Larregue Marc
Department of Dermatology, CHU la Milétrie, Poitiers Cedex, France.
Pediatr Dermatol. 2005 Sep-Oct;22(5):412-4. doi: 10.1111/j.1525-1470.2005.00104.x.
Seven patients with bi-acromial dimples are reported, with a family history in only one. This skin condition presented as an anatomic peculiarity without associated abnormalities. Although it has been previously documented as a finding in malformation syndromes such as the 18q syndrome, we point out that it may be found quite frequently in isolation and without morbidity. Therefore, it should be mainly considered as an anatomic variation without pathologic significance.
报告了7例有双侧肩峰酒窝的患者,其中只有1例有家族史。这种皮肤状况表现为一种解剖学上的特殊现象,无相关异常。尽管它先前已被记录为诸如18q综合征等畸形综合征中的一种表现,但我们指出,它可能经常单独出现且无病态。因此,应主要将其视为一种无病理意义的解剖学变异。