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Hereditary spastic paraplegia and extensive leukoencephalopathy: a case report of a unique phenotype associated with a GJB1/Cx32 p.Pro174Ser variant

Published Online: 2024-09-04

Authors

Nakamura, Haruko

Doi, Hiroshi

Miyaji, Yosuke

Wada, Taishi

Takahashi, Erisa

Tada, Mikiko

Fukuda, Hiromi

Fujita, Atsushi

Higashiyama, Yuichi

Nagao, Yuri

Kimura, Kazue

Hayashi, Masaharu

Hoshino, Kyoko

Matsumoto, Naomichi

Tanaka, Fumiaki
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Text and Data Mining valid from 2024-09-04

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Article History

Received: 22 June 2024

Accepted: 26 August 2024

First Online: 4 September 2024

Declarations

:

: Research protocols were approved by the Institutional Review Board of Yokohama City University School of Medicine (A130530002), and written informed consent was obtained from all patients.

: Written informed consent for publication was obtained from all patients.

: The authors declare no competing interests.

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