Biallelic CPAMD8 variants in a patient with ectopia lentis associated with extraocular systemic features reminiscent of Marfan syndrome
Here we report an 18-year-old male patient with bilateral ectopia lentis and biallelic CPAMD8 variants (NM_015692.5:c.[2801delG];[4552C>T]; NP_056507.3:p.[(Gly934GlufsTer64)];[(Gln1518Ter)]). He exhibited previously unreported extraocular features, including a slender build, scoliosis, arachnodactyly and positive thumb sign and wrist sign, which is reminiscent of Marfan syndrome. These findings may suggest that CPAMD8-related disorder is a syndromic condition associated with extraocular systemic features similar to those seen in Marfan syndrome.
Authors
- Keiji Hasumi (ORCID: https://orcid.org/0000-0002-3340-7312)
- Masaya Fukushima (ORCID: https://orcid.org/0000-0001-9485-4653)
- Daiju Oba (ORCID: https://orcid.org/0000-0002-8184-7742)
- Masaaki Sagara
- Hirofumi Ohashi (ORCID: https://orcid.org/0009-0008-2709-3186)
- S. Oda (ORCID: https://orcid.org/0000-0001-5836-768X)
Institutions
- Saitama Children's Medical Center (JP)
Publication Details
- Journal
- Human Genome Variation
- Published
- 2025-10-27
- DOI
- https://doi.org/10.1038/s41439-025-00329-9
- Primary Topic
- Connective tissue disorders research
- Type
- article
- Field-Weighted Citation Impact
- 0.00