McBurney E I, Christianson H B, Smith W B
J Am Acad Dermatol. 1979 Sep;1(3):240-3. doi: 10.1016/s0190-9622(79)70016-8.
A 7-year-old white boy had multiple angiokeratomas, connective tissue nevus of the right foot, and cavernous hemangioma with hemiatrophy of the right lower extremity. The triad of abnormalities is distinct from previously described multiple malformation syndromes.
一名7岁白人男孩患有多发性血管角化瘤、右脚结缔组织痣以及伴有右下肢半侧萎缩的海绵状血管瘤。这一三联征异常不同于先前描述的多种畸形综合征。