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A Case of Sjogren-Larsson Syndrome
Journal of the Korean Ophthalmological Society ; : 1605-1609, 1995.
Article in Korean | WPRIM | ID: wpr-172475
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.
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Full text: Available Index: 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 Type: Article

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Full text: Available Index: 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 Type: Article