Sela B A, Massos T, Fogel D, Zlotnik J
Pathological Chemistry Institute, Sheba Medical Center, Tel Hashomer.
Harefuah. 1999 Nov 15;137(10):451-3, 511.
A 3.5-year-old boy with developmental motor retardation, hypotonicity, and severe speech disturbance had alpha-amino adipic acid in his blood and very high levels in his urine. In only 20 cases has this catabolite of lysine and hydroxylysine been found in high concentrations in urine, due to enzymatic block. The clinical features associated with alpha-amino adipic aciduria may include mental retardation, developmental and motor delay, learning difficulties, convulsions, speech problems and ataxia. 3 siblings had milder symptoms of psychomotor delay and intermediate degrees of alpha amino-adipic aciduria, suggesting that the described developmental deficits could be related to this metabolite or its derivatives.
一名3.5岁男孩患有发育性运动迟缓、肌张力减退和严重语言障碍,其血液中含有α-氨基己二酸,尿液中含量极高。由于酶阻断,仅在20例病例中发现这种赖氨酸和羟赖氨酸的分解代谢产物在尿液中浓度很高。与α-氨基己二酸尿症相关的临床特征可能包括智力发育迟缓、发育和运动延迟、学习困难、惊厥、言语问题和共济失调。3名兄弟姐妹有较轻的精神运动发育迟缓症状和中度的α-氨基己二酸尿症,这表明所描述的发育缺陷可能与这种代谢产物或其衍生物有关。