P328: When 'X' does not mark the spot: A surviving male with incontinentia pigmenti
Abstract
The patient is followed within a multidisciplinary program involving Dermatology, Clinical Genomics, Ophthalmology, Neurology and Dentistry. Dermatologic lesions have continued to evolve along the expected IP stages within a predictable time course. Ophthalmology managed the retinal vasculopathy with photocoagulation. Close surveillance by our Ophthalmology colleagues is ongoing to monitor for neovascularization or retinal detachment. Neurology follows the patient for early detection of IP-associated seizures or other neurologic phenomena; to date, he has remained seizure-free.
Fields of Study & Subjects
Genetic and rare skin diseases.
Skin and Cellular Biology Research
Genomics and Rare Diseases
Publication details
- Journal / source
- Genetics in Medicine Open
- Volume
- 4
- Pages
- 103822–103822
- Publication date
- 1 January 2026
- Language
- EN