Edwards M J, McDonald D, Moore P, Rae J
Newcastle and Northern New South Wales Genetics Service, Tamworth Base Hospital and Health Service, Australia.
Am J Med Genet. 1994 Apr 15;50(3):247-50. doi: 10.1002/ajmg.1320500307.
Scalp-ear-nipple (SEN) syndrome is a rare, autosomal dominant condition that causes aplasia cutis congenita of the scalp, alteration of the shape of the external ear, and hypoplasia of the nipple. Women in a new family, the fifth to be described, had virtually complete aplasia of the breast and a small skin dimple without any pigmentation instead of a normal nipple, although other affected women had normal breast and nipple development. Dental changes included widely spaced or missing secondary teeth; the ears were cupped or folded and stood out from the head, axillary apocrine secretion and axillary hair growth were reduced; and finger nails were brittle. There was no generalized abnormality of sweating. Some patients had partial syndactyly of the 3rd and 4th fingers, and complete cutaneous syndactyly of the 2nd and 3rd toes. and 3rd toes.
头皮-耳-乳头(SEN)综合征是一种罕见的常染色体显性疾病,可导致头皮先天性皮肤发育不全、外耳形状改变和乳头发育不全。在新报道的第五个家系中,患病女性几乎完全没有乳房组织,仅有一个无色素沉着的小皮肤凹陷,而非正常乳头,不过其他患病女性的乳房和乳头发育正常。牙齿变化包括恒牙间隙过宽或缺失;耳朵呈杯状或折叠状,突出于头部,腋窝顶泌汗腺分泌和腋毛生长减少;指甲易碎。无全身性出汗异常。部分患者第3和第4指有部分并指,第2和第3趾有完全性皮肤并指。