Department of Pediatrics and Amsterdam Lysosome Center Sphinx, Academic Medical Center, University of Amsterdam, Amsterdam, The Netherlands.
J Inherit Metab Dis. 2010 Dec;33(6):759-67. doi: 10.1007/s10545-010-9199-y. Epub 2010 Sep 18.
Mucopolysaccharidosis type IIIB (MPS IIIB, Sanfilippo syndrome type B) is a lysosomal storage disorder caused by deficiency of the enzyme N-acetyl-α-D-glucosaminidase (NAGLU). Information on the natural course of MPS IIIB is scarce but much needed in view of emerging therapies. To improve knowledge on the natural course, data on all 52 MPS IIIB patients ever identified by enzymatic studies in the Netherlands were gathered. Clinical data on 44 patients could be retrieved. Only a small number (n = 9; 21%) presented with a classical MPS III phenotype; all other patients showed a much more attenuated course of the disease characterized by a significantly slower regression of intellectual and motor abilities. The majority of patients lived well into adulthood. First signs of the disease, usually mild developmental delay, were observed at a median age of 4 years. Subsequently, patients showed a slowing and eventually a stagnation of development. Patients with the attenuated phenotype had a stable intellectual disability for many years. Molecular analysis was performed in 24 index patients. The missense changes p.R643C, p.S612G, p.E634K, and p.L497V were exclusively found in patients with the attenuated phenotype. MPS IIIB comprises a remarkably wide spectrum of disease severity, and an unselected cohort including all Dutch patients showed a large proportion (79%) with an attenuated phenotype. MPS IIIB must be considered in patients with a developmental delay, even in the absence of a progressive decline in intellectual abilities. A key feature, necessitating metabolic studies, is the coexistence of behavioral problems.
黏多糖贮积症 IIIB 型(MPS IIIB,Sanfilippo 综合征 B 型)是一种溶酶体贮积病,由 N-乙酰-α-D-氨基葡萄糖苷酶(NAGLU)缺乏引起。鉴于新兴疗法的出现,对 MPS IIIB 自然病程的信息需求迫切,但目前却十分匮乏。为了深入了解自然病程,我们收集了荷兰通过酶学研究确定的所有 52 例 MPS IIIB 患者的临床资料。其中 44 例患者的临床数据可以检索到。仅有一小部分(n=9;21%)表现为典型的 MPS III 表型;其余所有患者的疾病进展都更为缓和,智力和运动能力的衰退速度显著较慢。大多数患者可进入成年期。大多数患者在中位年龄 4 岁时出现首发症状,通常为轻度发育迟缓。随后,患者的发育逐渐减慢,最终停滞。具有缓和表型的患者在智力障碍方面会保持稳定多年。对 24 例索引患者进行了分子分析。在具有缓和表型的患者中,仅发现错义改变 p.R643C、p.S612G、p.E634K 和 p.L497V。MPS IIIB 表现出显著的疾病严重程度谱,包括所有荷兰患者在内的未选择队列中有很大一部分(79%)表现出缓和表型。在没有智力能力进行性下降的情况下,出现发育迟缓的患者都应考虑 MPS IIIB 的可能。一个关键特征是需要代谢研究,即同时存在行为问题。