Please use this identifier to cite or link to this item: https://doi.org/10.1212/NXG.0000000000000345
Title: Novel mutation in HTRA1 in a family with diffuse white matter lesions and inflammatory features
Authors: Ziaei, A.
Xu, X.
Dehghani, L.
Bonnard, C.
Zellner, A.
Ng, A.Y.J.
Tohari, S.
Venkatesh, B. 
Haffner, C.
Reversade, B.
Shaygannejad, V.
Pouladi, M.A. 
Issue Date: 2019
Publisher: Lippincott Williams and Wilkins
Citation: Ziaei, A., Xu, X., Dehghani, L., Bonnard, C., Zellner, A., Ng, A.Y.J., Tohari, S., Venkatesh, B., Haffner, C., Reversade, B., Shaygannejad, V., Pouladi, M.A. (2019). Novel mutation in HTRA1 in a family with diffuse white matter lesions and inflammatory features. Neurology: Genetics 5 (4) : 345. ScholarBank@NUS Repository. https://doi.org/10.1212/NXG.0000000000000345
Rights: Attribution-NonCommercial-NoDerivatives 4.0 International
Abstract: Objective To investigate the possible involvement of germline mutations in a neurologic condition involving diffuse white matter lesions. Methods The patients were 3 siblings born to healthy parents. We performed homozygosity mapping, whole-exome sequencing, site-directed mutagenesis, and immunoblotting. Results All 3 patients showed clinical manifestations of ataxia, behavioral and mood changes, premature hair loss, memory loss, and lower back pain. In addition, they presented with inflammatory-like features and recurrent rhinitis. MRI showed abnormal diffuse demyelination lesions in the brain and myelitis in the spinal cord. We identified an insertion in high-temperature requirement A (HTRA1), which showed complete segregation in the pedigree. Functional analysis showed the mutation to affect stability and secretion of truncated protein. Conclusions The patients’ clinical manifestations are consistent with cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy (CARASIL; OMIM #600142), which is known to be caused by HTRA1 mutations. Because some aspects of the clinical presentation deviate from those reported for CARASIL, our study expands the spectrum of clinical consequences of loss-of-function mutations in HTRA1. Copyright © 2019 The Author(s).
Source Title: Neurology: Genetics
URI: https://scholarbank.nus.edu.sg/handle/10635/209949
ISSN: 2376-7839
DOI: 10.1212/NXG.0000000000000345
Rights: Attribution-NonCommercial-NoDerivatives 4.0 International
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