A Clinical Neurological Approach to the Child With Adenosine Deaminase Deficiency

IF 3.2 3区 医学 Q2 CLINICAL NEUROLOGY
Paula Ivarola MD , Luciano Urdinez MD , Matias Oleastro MD , Danila Labonia MD , Mariana Roizen MD , Roberto Caraballo MD , Silvia Tenembaum MD
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Abstract

Background

Severe combined immunodeficiency secondary to adenosine deaminase deficiency is rare. The deficiency of this enzyme results in the accumulation of substrates in the tissues, including the brain. Clinical signs of neurological involvement may include seizures, neurodevelopmental disorders, hypotonia, and sensorineural hearing loss. Hematopoietic stem cell transplantation corrects the failure of the immune system but not the neurological involvement.

Objectives

To describe the spectrum of neurological complications identified in a series of children with severe combined immunodeficiency due to adenosine deaminase deficiency. Additionally, we propose a neurological approach including electrophysiological, radiological, and neurocognitive studies to address this group of children in an efficient and timely manner.

Methods

A descriptive, observational, retro-, and prospective analysis of patients with a confirmed immunological diagnosis seen between 1996 and 2021 and referred to the Department of Neurology for neurological evaluation was conducted.

Results

Ten patients met the inclusion criteria. The median age at diagnosis was 4 months (range, 1-36 months). All patients had neurodevelopmental delay with hypotonia in six, language delay in three, sensorineural hearing loss in four, and spastic paraparesis in one patient. Two children developed an epileptic syndrome, consisting of generalized epilepsy in one and focal epilepsy in the other. Neuroimaging showed brain calcifications in the basal ganglia and/or centrum semiovale in four patients and enlarged subarachnoid spaces in two other patients.

Conclusion

In this pediatric series, the rate of neurological involvement associated with abnormalities on neuroimaging was high. Although this involvement could be related to accumulation of adenosine metabolites in the central nervous system, the possibility of associated chronic infections should be ruled out. Given the neurological manifestations, it is important to involve the pediatric neurologist in the multidisciplinary follow-up team.

腺苷脱氨酶缺乏症患儿的临床神经学方法
背景继发于腺苷脱氨酶缺乏症的严重联合免疫缺陷症非常罕见。这种酶的缺乏会导致底物在包括大脑在内的组织中蓄积。神经系统受累的临床表现可能包括癫痫发作、神经发育障碍、肌张力低下和感音神经性听力损失。造血干细胞移植可纠正免疫系统的衰竭,但不能纠正神经系统的受累。此外,我们还提出了一种包括电生理学、放射学和神经认知研究在内的神经学方法,以高效、及时地解决这类患儿的问题。方法对 1996 年至 2021 年期间确诊为免疫缺陷并转诊至神经内科进行神经学评估的患者进行描述性、观察性、追溯性和前瞻性分析。确诊时的中位年龄为 4 个月(1-36 个月)。所有患者均有神经发育迟缓症状,其中 6 名患者肌张力低下,3 名患者语言发育迟缓,4 名患者感音神经性听力损失,1 名患者痉挛性瘫痪。两名患儿出现了癫痫综合征,其中一人患有全身性癫痫,另一人患有局灶性癫痫。神经影像学检查显示,四名患者的基底节和/或半卵圆中心出现脑钙化,另外两名患者的蛛网膜下腔扩大。虽然这种受累可能与腺苷代谢产物在中枢神经系统的蓄积有关,但也应排除相关慢性感染的可能性。考虑到神经系统的表现,让小儿神经科医生加入多学科随访小组非常重要。
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来源期刊
Pediatric neurology
Pediatric neurology 医学-临床神经学
CiteScore
4.80
自引率
2.60%
发文量
176
审稿时长
78 days
期刊介绍: Pediatric Neurology publishes timely peer-reviewed clinical and research articles covering all aspects of the developing nervous system. Pediatric Neurology features up-to-the-minute publication of the latest advances in the diagnosis, management, and treatment of pediatric neurologic disorders. The journal''s editor, E. Steve Roach, in conjunction with the team of Associate Editors, heads an internationally recognized editorial board, ensuring the most authoritative and extensive coverage of the field. Among the topics covered are: epilepsy, mitochondrial diseases, congenital malformations, chromosomopathies, peripheral neuropathies, perinatal and childhood stroke, cerebral palsy, as well as other diseases affecting the developing nervous system.
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