Robb S A, Pohl K R, Baraitser M, Wilson J, Brett E M
Hospital for Sick Children, London.
Arch Dis Child. 1989 Jan;64(1):83-6. doi: 10.1136/adc.64.1.83.
Thirty six children with typical features of Angelman's syndrome, including global developmental delay, ataxia, episodes of paroxysmal laughter, seizures, and microcephaly were studied. The series included three sibships of three affected sisters, two affected brothers, and two affected sisters, respectively. The facial appearance is characterised by a prominent jaw, a wide mouth, and a pointed chin. Tongue thrusting is common. The movement disorder consists of a wide based, ataxic gait with frequent jerky limb movements and flapping of the hands. Tone is variable in the limbs with normal reflexes, and the plantar responses are usually flexor. The syndrome is being diagnosed more often, and attention is drawn to its diagnostic aspects.
对36名患有天使综合征典型特征的儿童进行了研究,这些特征包括全面发育迟缓、共济失调、阵发性大笑发作、癫痫发作和小头畸形。该系列分别包括三个患病姐妹、两个患病兄弟和两个患病姐妹的三个同胞组。面部特征为下颌突出、嘴巴宽阔、下巴尖锐。伸舌常见。运动障碍表现为宽基、共济失调步态,伴有频繁的肢体急促运动和手部扑动。四肢肌张力可变,反射正常,跖反射通常为屈性。该综合征的诊断越来越频繁,人们也开始关注其诊断方面。