A case of retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations: Long‐term treatment with repeated courses of immunotherapy

Muguruma, Kazuki; Sugimoto, Takamichi; Terada, Yoshiko; Yuan, Jun‐Hui; Nomura, Eiichi; Takashima, Hiroshi; Yamawaki, Takemori; Kohriyama, Tatsuo; Makino, Hírofumi

doi:10.1111/ncn3.12664

Neurology & Clinical Neurosc

2022

DOI: 10.1111/ncn3.12664

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A case of retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations: Long‐term treatment with repeated courses of immunotherapy

Kazuki Muguruma

Takamichi Sugimoto

Yoshiko Terada

et al.

Abstract: RVCL-S is a hereditary disease caused by a heterozygous mutation in the TREX1 gene. 1 We report the case of an RVCL-S patient who underwent repeated rounds of immunotherapy.

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A case of retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations: Long‐term treatment with repeated courses of immunotherapy

Abstract: RVCL-S is a hereditary disease caused by a heterozygous mutation in the TREX1 gene. 1 We report the case of an RVCL-S patient who underwent repeated rounds of immunotherapy.

Cited by 0 publications

References 12 publications

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