Department of Neurology, Mayo Clinic, 4500 San Pablo Rd S, Jacksonville, FL, 32224, USA.
Division of Neurological and Psychiatric Nursing, Faculty of Health Sciences, Medical University of Gdansk, Gdansk, 80-211, Poland.
Orphanet J Rare Dis. 2023 Jun 22;18(1):160. doi: 10.1186/s13023-023-02772-9.
CSF1R mutations cause autosomal-dominant CSF1R-related leukoencephalopathy with axonal spheroids and pigmented glia (CSF1R-ALSP) and autosomal-recessive brain abnormalities, neurodegeneration, and dysosteosclerosis (BANDDOS). The former is increasingly recognized, and disease-modifying therapy was introduced; however, literature is scarce on the latter. This review analyzes BANDDOS and discusses similarities and differences with CSF1R-ALSP.We systematically retrieved and analyzed the clinical, genetic, radiological, and pathological data on the previously reported and our cases with BANDDOS. We identified 19 patients with BANDDOS (literature search according to the PRISMA 2020 guidelines: n = 16, our material: n = 3). We found 11 CSF1R mutations, including splicing (n = 3), missense (n = 3), nonsense (n = 2), and intronic (n = 2) variants and one inframe deletion. All mutations disrupted the tyrosine kinase domain or resulted in nonsense-mediated mRNA decay. The material is heterogenous, and the presented information refers to the number of patients with sufficient data on specific symptoms, results, or performed procedures. The first symptoms occurred in the perinatal period (n = 5), infancy (n = 2), childhood (n = 5), and adulthood (n = 1). Dysmorphic features were present in 7/17 cases. Neurological symptoms included speech disturbances (n = 13/15), cognitive decline (n = 12/14), spasticity/rigidity (n = 12/15), hyperactive tendon reflex (n = 11/14), pathological reflexes (n = 8/11), seizures (n = 9/16), dysphagia (n = 9/12), developmental delay (n = 7/14), infantile hypotonia (n = 3/11), and optic nerve atrophy (n = 2/7). Skeletal deformities were observed in 13/17 cases and fell within the dysosteosclerosis - Pyle disease spectrum. Brain abnormalities included white matter changes (n = 19/19), calcifications (n = 15/18), agenesis of corpus callosum (n = 12/16), ventriculomegaly (n = 13/19), Dandy-Walker complex (n = 7/19), and cortical abnormalities (n = 4/10). Three patients died in infancy, two in childhood, and one case at unspecified age. A single brain autopsy evidenced multiple brain anomalies, absence of corpus callosum, absence of microglia, severe white matter atrophy with axonal spheroids, gliosis, and numerous dystrophic calcifications.In conclusion, BANDDOS presents in the perinatal period or infancy and has a devastating course with congenital brain abnormalities, developmental delay, neurological deficits, osteopetrosis, and dysmorphic features. There is a significant overlap in the clinical, radiological, and neuropathological aspects between BANDDOS and CSF1R-ALSP. As both disorders are on the same continuum, there is a window of opportunity to apply available therapy in CSF1R-ALSP to BANDDOS.
CSF1R 突变导致常染色体显性 CSF1R 相关脑白质病伴轴索性球体和色素性神经胶质(CSF1R-ALSP)和常染色体隐性脑异常、神经退行性变和骨硬化症(BANDDOS)。前者越来越受到重视,已经引入了疾病修饰疗法;然而,关于后者的文献却很少。本文分析了 BANDDOS,并讨论了其与 CSF1R-ALSP 的相似之处和不同之处。
我们系统地检索并分析了以前报道的和我们的 BANDDOS 病例的临床、遗传、放射学和病理学数据。我们确定了 19 名 BANDDOS 患者(根据 PRISMA 2020 指南进行文献检索:n=16,我们的资料:n=3)。我们发现了 11 种 CSF1R 突变,包括剪接(n=3)、错义(n=3)、无义(n=2)和内含子(n=2)变体以及一个框内缺失。所有突变均破坏了酪氨酸激酶结构域或导致无义介导的 mRNA 衰变。该材料存在异质性,并且呈现的信息是指特定症状、结果或已进行的程序具有足够数据的患者数量。首发症状发生在围产期(n=5)、婴儿期(n=2)、儿童期(n=5)和成年期(n=1)。7/17 例存在畸形特征。神经症状包括言语障碍(n=13/15)、认知能力下降(n=12/14)、痉挛/僵硬(n=12/15)、腱反射亢进(n=11/14)、病理性反射(n=8/11)、癫痫发作(n=9/16)、吞咽困难(n=9/12)、发育迟缓(n=7/14)、婴儿期张力减退(n=3/11)和视神经萎缩(n=2/7)。13/17 例观察到骨骼畸形,属于骨硬化症-皮勒病谱。脑部异常包括白质变化(n=19/19)、钙化(n=15/18)、胼胝体发育不全(n=12/16)、脑室扩大(n=13/19)、Dandy-Walker 复合体(n=7/19)和皮质异常(n=4/10)。3 名患者在婴儿期死亡,2 名在儿童期死亡,1 名在未指明的年龄死亡。一例单一的脑部尸检显示存在多个脑部异常,胼胝体缺失,小胶质细胞缺失,白质严重萎缩伴轴索性球体,神经胶质增生和大量营养不良性钙化。
总之,BANDDOS 发生在围产期或婴儿期,具有毁灭性的病程,伴有先天性脑异常、发育迟缓、神经功能缺损、骨质硬化症和畸形特征。BANDDOS 和 CSF1R-ALSP 在临床、放射学和神经病理学方面有显著的重叠。由于这两种疾病处于同一连续体上,因此有机会将 CSF1R-ALSP 中可用的治疗方法应用于 BANDDOS。