A Case of Sjogren-Larsson Syndrome
Journal of the Korean Ophthalmological Society
; : 1605-1609, 1995.
Article
in Korean
| WPRIM (Western Pacific)
| ID: wpr-172475
Responsible library:
WPRO
ABSTRACT
The Sjogren-Larsson syndrome is genetically determined syndrome with autosomal recessive inheritence and characterized by the three cardinal signs congenital ichthyosis, spastic di/tetraplegia, and mental retardation. Ocular signs include ectropion, blepharitis, conjunctivitis, keratitis, and macular glistening spot. The authors have experienced a case of Sjogren-Larsson syndrome that showed classical triad and macular glistening spot in a 16 month old boy.
Full text:
Available
Database:
WPRIM (Western Pacific)
Main subject:
Blepharitis
/
Sjogren-Larsson Syndrome
/
Conjunctivitis
/
Ectropion
/
Ichthyosis
/
Keratitis
/
Intellectual Disability
/
Muscle Spasticity
Limits:
Humans
/
Infant
/
Male
Language:
Korean
Journal:
Journal of the Korean Ophthalmological Society
Year:
1995
Document type:
Article
