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Sjogren-Larsson Syndrome

Known as: ICHTHYOSIS, SPASTIC NEUROLOGIC DISORDER, AND OLIGOPHRENIA, Sjogren Larsson syndrome, Sjögren-Larsson Syndrome 
An autosomal recessive neurocutaneous disorder characterized by severe ichthyosis MENTAL RETARDATION; SPASTIC PARAPLEGIA; and congenital ICHTHYOSIS… 
National Institutes of Health

Related topics

Related topics

18 relations
Autosomal recessive inheritanceCentral nervous system demyelinationCongenital ichthyosisDental Enamel Hypoplasia

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Sjogren-Larsson-like syndrome

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2006
Highly Cited
2006
Restoration of fatty aldehyde dehydrogenase deficiency in Sjögren–Larsson syndrome
Sjögren–Larsson syndrome (SLS) is an autosomal recessive neurocutaneous disorder caused by mutation in the ALDH3A2 gene that… 
2006
2006
Phenotypic variability among adult siblings with Sjögren-Larsson syndrome.
BACKGROUND Sjögren-Larsson syndrome (SLS) is an early childhood-onset disorder with ichthyosis, mental retardation, spastic… 
2004
2004
Moderate skin sensitizers can induce phenotypic changes on in vitro generated dendritic cells.
2000
2000
5-Lipoxygenase inhibition: a new treatment strategy for Sjögren-Larsson syndrome.
The Sjögren-Larsson syndrome (SLS) is a severe neurocutaneous disorder due to fatty aldehyde dehydrogenase (FALDH) deficiency… 
Highly Cited
1999
Highly Cited
1999
Somatolactin in the white sturgeon and African lungfish and its evolutionary significance.
Somatolactin (SL) is a newly characterized pituitary hormone belonging to the growth hormone-prolactin family. Until now SL has… 
1996
1996
Cloning and expression of somatolactin, a pituitary hormone related to growth hormone and prolactin from gilthead seabream, Sparus aurata.
A pituitary hormone, somatolactin (SL), belonging to the GH/PRL family, is produced in the intermediate lobe of the teleost… 
Highly Cited
1991
Highly Cited
1991
Sjögren-Larsson syndrome. Deficient activity of the fatty aldehyde dehydrogenase component of fatty alcohol:NAD+ oxidoreductase in cultured fibroblasts.
Sjögren-Larsson syndrome (SLS) is an inherited disorder associated with impaired fatty alcohol oxidation due to deficient… 
1990
1990
Depletion of alcohol (hexanol) dehydrogenase activity in the epidermis and jejunal mucosa in Sjögren-Larsson syndrome.
Using a histochemical technique, we have demonstrated a consistent deficiency of alcohol (hexanol) dehydrogenase activity within… 
Highly Cited
1982
Highly Cited
1982
Ichthyosis in the Sjögren‐Larsson syndrome
The Sjögren‐Larsson syndrome (SLS) is characterized by congenital ichthyosis, spastic dior tetraplegia and mental retardation… 
1982
1982
Suspected Faulty Essential Fatty Acid Metabolism in Sjögren-Larsson Syndrome
The aim of the present study was to examine the fatty acid patterns of plasma phospholipids, cholesteryl esters, triglycerides… 
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