Clinical and molecular characterization and response to acitretin in three families with Sjögren-Larsson syndrome

Author:

Vural Seçil12ORCID,Vural Atay23,Akçimen Fulya4ORCID,Bağci Işın S.1,Tunca Ceren4,Gündoğdu Eken Asli4,Ruzicka Thomas1,Başak A. Nazli4

Affiliation:

1. Ludwig Maximillians University, Dermatology and Allergology; Munich Germany

2. Adıyaman Besni State Hospital; Adiyaman Turkey

3. Department of Neurology; Koç University; Istanbul Turkey

4. Suna and İnan Kıraç Foundation; Neurodegeneration Research Laboratory (NDAL); Boğaziçi University; Istanbul Turkey

Publisher

Wiley

Subject

Dermatology

Reference38 articles.

1. Sjogren-Larsson syndrome is caused by mutations in the fatty aldehyde dehydrogenase gene;Laurenzi;Nat Genet,1996

2. Microsomal fatty aldehyde dehydrogenase catalyzes the oxidation of aliphatic aldehyde derived from ether glycerolipid catabolism: implications for Sjogren-Larsson syndrome;Rizzo;Biochem Biophys Acta,2000

3. Ichthyosis in Sjogren-Larsson syndrome reflects defective barrier function due to abnormal lamellar body structure and secretion;Rizzo;Arch Dermatol Res,2010

4. Systemic treatment of pediatric psoriasis: a review;Napolitano;Dermatol Ther,2016

5. British Association of Dermatologists guidelines on the efficacy and use of acitretin in dermatology;Ormerod;Br J Dermatol,2010

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