Abstract
Setleis syndrome is a rare skin disorder characterized by congenital scar-like depressions on the temples and distinctive facial appearance. We report on two from a consanguineous Omani family, with typical features of this syndrome. The mother in one case has mild dysmorphic features reminiscent of this syndrome and the father of the other case has bitemporal scars only.
Original language | English |
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Pages (from-to) | 249-253 |
Number of pages | 5 |
Journal | Clinical Dysmorphology |
Volume | 5 |
Issue number | 3 |
Publication status | Published - 1996 |
Keywords
- Setleis syndrome
- autosomal dominant
- autosomal recessive
- consanguinity
ASJC Scopus subject areas
- Pediatrics, Perinatology, and Child Health
- Anatomy
- Pathology and Forensic Medicine
- Genetics(clinical)