Lynch D R, McDonald-McGinn D M, Zackai E H, Emanuel B S, Driscoll D A, Whitaker L A, Fischbeck K H
Department of Neurology, University of Pennsylvania School of Medicine, Philadelphia, USA.
J Med Genet. 1995 Jul;32(7):561-3. doi: 10.1136/jmg.32.7.561.
Velocardiofacial syndrome and DiGeorge syndrome have not previously been associated with central nervous system degeneration. We report a 34 year old man who presented for neurological evaluation with cerebellar atrophy of unknown aetiology. On historical review, he had neonatal hypocalcaemia, an atrial septal defect, and a corrected cleft palate. His physical examination showed the characteristic facies of velocardiofacial syndrome as well as dysmetria and dysdiadocho-kinesia consistent with cerebellar degeneration. Molecular cytogenetic studies showed a deletion of 22q11.2. This man is the first reported patient with the association of a neurodegenerative disorder and 22q11.2 deletion syndrome.
腭心面综合征和迪格奥尔格综合征此前并未被认为与中枢神经系统退变有关。我们报告一名34岁男性,因病因不明的小脑萎缩前来接受神经学评估。回顾病史,他曾患新生儿低钙血症、房间隔缺损和矫正腭裂。体格检查显示其具有腭心面综合征的典型面容,以及与小脑退变相符的辨距不良和轮替运动障碍。分子细胞遗传学研究显示22q11.2缺失。该男子是首例报告的患有神经退行性疾病与22q11.2缺失综合征关联的患者。