Renfree Kevin J, Dell Paul C
Department of Orthopedics, Mayo Clinic Hospital, Phoenix, AZ.
Department of Orthopaedic Surgery and Hand and Upper Extremity Division, University of Florida, Gainesville, FL.
J Hand Surg Am. 2016 Jul;41(7):e207-10. doi: 10.1016/j.jhsa.2016.04.014. Epub 2016 May 10.
Adams-Oliver syndrome is a rare congenital condition that should be considered in persons with terminal transverse limb deficiencies and scalp defects (aplasia cutis congenita). Broad phenotypic variability exists in this condition. In its more severe forms, Adams-Oliver syndrome can involve the cardiovascular system, central nervous system, gastrointestinal tract, and genitourinary system and should require prompt evaluation by appropriate subspecialists. Extremity involvement is typically bilateral and asymmetrical, with lower extremities involved more than upper extremities. Brachydactyly is the most common limb defect, and severity ranges from hypoplastic nails to complete absence of the distal limb. The syndrome has been described as resulting from autosomal dominant and recessive modes of inheritance, but most cases are sporadic. No gene has been identified. Although the exact pathogenic mechanism is unknown, a common hypothesis is that a vascular disturbance occurs in watershed areas, such as cranial vertex and limbs, during fetal development.
亚当斯-奥利弗综合征是一种罕见的先天性疾病,对于患有末端横向肢体缺损和头皮缺陷(先天性皮肤发育不全)的人应考虑此病。这种疾病存在广泛的表型变异。在其更严重的形式中,亚当斯-奥利弗综合征可累及心血管系统、中枢神经系统、胃肠道和泌尿生殖系统,应由相应的专科医生进行及时评估。肢体受累通常是双侧且不对称的,下肢比上肢更常受累。短指畸形是最常见的肢体缺陷,严重程度从指甲发育不全到远端肢体完全缺失不等。该综合征已被描述为常染色体显性和隐性遗传模式导致,但大多数病例是散发性的。尚未确定相关基因。尽管确切的致病机制尚不清楚,但一个常见的假说是在胎儿发育期间,诸如颅顶和四肢等分水岭区域发生了血管紊乱。