Partial Oculomotor Nerve Palsy Revealing PDCD10-Related Familial Cerebral Cavernous Malformation in a Child
Yoshimi Murakami, Takanobu Inoue, Shun Ishikura, Ryo Fujimoto, Hiromi Aoyama · 2026
Read Partial Oculomotor Nerve Palsy Revealing PDCD10-Related Familial Cerebral Cavernous Malformation in a Child by Yoshimi Murakami, Takanobu Inoue, Shun Ishikura, Ryo Fujimoto, Hiromi Aoyama (2026) in the Tower of Babel, a free online library of public-domain works preserved in clean, searchable text. No sign-up. The full text is served as a plain-text file at a predictable URL, where text is present: https://antarctic-labs.com/tower-of-babel/PMC13392410.txt.
Description
Yoshimi Murakami and co-authors describe a toddler whose drooping right eyelid and limited eye movement turned out to be the first sign of an inherited brain vessel disorder. Genetic testing found a new variant in PDCD10, the gene tied to the most severe form of familial cerebral cavernous malformation. The report appeared in 2026.
Scans first showed many calcified spots in the brain, and magnetic resonance imaging then revealed multiple cavernous malformations. Follow-up imaging a year later showed fresh lesions, including one near the pons, plus bleeding beside the nerve that moves the eye. Because new lesions can appear quickly and bleeding risk stays high, the authors stress close monitoring over time.
Catalog record
| CREATOR | Yoshimi Murakami, Takanobu Inoue, Shun Ishikura, Ryo Fujimoto, Hiromi Aoyama |
|---|---|
| YEAR | 2026 |
| COLLECTION | PAPERS |
| FORMAT | TXT |
| FILE SIZE | 12814 |
| LICENSE | https://creativecommons.org/licenses/by/4.0 |
| RIGHTS | CC BY |
| SOURCE | Europe PMC |