Abstract
The nevus sebaceous of Jadassohn (NSJ) syndrome is a not uncommon pediatric dermatosis, with malignant potential. It is the cutaneous manifestation of another phakomatosis, characterized by neurologic, ophthalmic, cardiovascular, skeletal, and urogenital involvement. The features of this syndrome overlap those of the oculo-auriculo-vertebral dysplasia of Goldenhar and tuberous sclerosis. The extent of system involvement suggests a developmental insult during the first few weeks of gestation. A clearly genetic basis has not been established. An infant with NSJ syndrome is described who had associated optic nerve hypoplasia. His clinical, pathologic, and radiologic findings, including computed tomography (CT) and magnetic resonance imaging, are presented.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 1570-1576 |
| Number of pages | 7 |
| Journal | Ophthalmology |
| Volume | 94 |
| Issue number | 12 |
| DOIs | |
| State | Published - 1987 |
| Externally published | Yes |
Keywords
- linear nevus sebaceous syndrome of Jadassohn
- linear nevus syndrome
- optic nerve hypoplasia
- phakomatosis
ASJC Scopus subject areas
- Ophthalmology
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