N-methyl-d-aspartate (NMDA) receptor antibodies encephalitis mimicking an autistic regression

被引:33
|
作者
Hacohen, Yael [1 ,2 ]
Wright, Sukhvir [1 ,3 ]
Gadian, Jonathan [2 ]
Vincent, Angela [1 ]
Lim, Ming [2 ]
Wassmer, Evangeline [3 ]
Lin, Jean-Pierre [2 ]
机构
[1] Univ Oxford, Nuffield Dept Clin Neurosci, John Radcliffe Hosp, Oxford, England
[2] Guys & St Thomas NHS Fdn Trust, Paediat Neurosci, Evelina Childrens Hosp, Kings Hlth Partners Acad Hlth Sci Ctr, London, England
[3] Birmingham Childrens Hosp, Dept Paediat Neurol, Birmingham, W Midlands, England
来源
关键词
MOVEMENT-DISORDER; GRIN2A MUTATIONS; CHILDREN; ENCEPHALOPATHIES; EPILEPSY; APHASIA; DISEASE;
D O I
10.1111/dmcn.13169
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Expressive dysphasia and mutism are common clinical features in children and adults with N-methyl-d-aspartate receptor antibodies (NMDAR-Ab) encephalitis, and are likely to result from NMDAR hypofunction. A prodromal loss of social and communication skills can typify that of an autistic regression, particularly when presenting under the age of 3 years. Here we describe two toddlers who presented with developmental regression, particularly of their social communication skills, mimicking an autistic regression, who were found to have NMDAR-Ab in the serum and cerebrospinal fluid. Although both patients had some other neurological features, they were subtle, which resulted in delayed diagnosis of NMDAR-Ab encephalitis. Importantly, immunotherapy was beneficial in both patients, with significant improvement of their language skills and behaviour.
引用
收藏
页码:1092 / 1094
页数:3
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