Cutis Verticis Gyrata in <i>SPG11</i> ‐Related Hereditary Spastic Paraplegia: A Potential Novel Association
The data that support the findings of this study are available from the corresponding author upon reasonable request. Figure S1. Pedigree demonstrating parental consanguinity and two affected brothers, consistent with presumed autosomal recessive inheritance. The arrow indicates the proband. Created in BioRender. Coutinho, L. (2026). https://BioRender.com/xk8fsk1. Table S1. Comparison of reported cases of cutis verticis gyrata associated with spastic paraplegia. Please note: The publisher is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing content) should be directed to the corresponding author for the article.
Authors
- Salmo Raskin (ORCID: https://orcid.org/0000-0002-7191-0592)
- Patrícia Áurea Andreucci Martins Bonilha (ORCID: https://orcid.org/0000-0002-3397-3111)
- Luiz Eduardo Novis (ORCID: https://orcid.org/0000-0003-1479-2953)
- Hélio Afonso Ghizoni Teive (ORCID: https://orcid.org/0000-0003-2305-1073)
- Thabata Emanuelle Martins Nunes (ORCID: https://orcid.org/0000-0002-6789-0816)
- Léo Coutinho (ORCID: https://orcid.org/0000-0003-4921-2939)
- Walter O. Arruda (ORCID: https://orcid.org/0000-0002-2233-2183)
- Beatriz Cassarotti (ORCID: https://orcid.org/0000-0003-1655-4350)
Institutions
- Genetikum (DE)
- Hospital de Clínicas Universidade Federal do Paraná (BR)
- Universidade Federal do Paraná (BR)
Publication Details
- Journal
- Movement Disorders Clinical Practice
- Published
- 2026-06-26
- DOI
- https://doi.org/10.1002/mdc3.70718
- Primary Topic
- Hypertrophic osteoarthropathy and related conditions
- Type
- article
- Field-Weighted Citation Impact
- 0.00