Farrell S A, Warda L J, LaFlair P, Szymonowicz W
Division of Genetics, Credit Valley Hospital, Mississauga, Ontario, Canada.
Am J Med Genet. 1993 Dec 1;47(8):1175-9. doi: 10.1002/ajmg.1320470809.
We report on a patient with Adams-Oliver syndrome and report new findings: a chylous pleural effusion and juvenile chronic myelogenous leukemia. Also, our patient had congenital heart disease, confirming that heart lesions are a manifestation in this syndrome. The major manifestations of this disorder are summarized. Included are cases not previously recognized as having Adams-Oliver syndrome identified in a literature survey. Distal limb deficiency is commonest with more frequent and more severe involvement of the lower limbs. Scalp defects are the second commonest manifestation, while an underlying skull defect is not infrequent. Cutis marmorata telangiectatica and dilated scalp veins are significant signs of this condition. This review highlights unresolved questions about Adams-Oliver syndrome.
我们报告了一例患有亚当斯-奥利弗综合征的患者,并报告了新的发现:乳糜性胸腔积液和青少年慢性粒细胞白血病。此外,我们的患者患有先天性心脏病,证实心脏病变是该综合征的一种表现。总结了该疾病的主要表现。其中包括在文献调查中发现的以前未被确认为患有亚当斯-奥利弗综合征的病例。肢体远端缺损最为常见,下肢受累更频繁且更严重。头皮缺损是第二常见的表现,而潜在的颅骨缺损并不少见。大理石样皮肤毛细血管扩张症和头皮静脉扩张是该病症的重要体征。本综述强调了关于亚当斯-奥利弗综合征尚未解决的问题。