Sjögren‐Larsson syndrome: The mild end of the phenotypic spectrum

Sjögren‐Larsson syndrome (SLS) is a rare inborn error of lipid metabolism. The syndrome is caused by mutations in the ALDH3A2 gene, resulting in a deficiency of fatty aldehyde dehydrogenase. Most patients have a clearly recognizable severe phenotype, with congenital ichthyosis, intellectual disabili...

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Detalles Bibliográficos
Autores principales: Staps, Pippa, van Gaalen, Judith, van Domburg, Peter., Steijlen, Peter M., Ferdinandusse, Sacha, den Heijer, Tom, Seyger, Marieke M. B., Theelen, Thomas, Willemsen, Michèl A. A. P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2020
Materias:
Research Reports
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7203653/
https://www.ncbi.nlm.nih.gov/pubmed/32395410
http://dx.doi.org/10.1002/jmd2.12099

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7203653/
https://www.ncbi.nlm.nih.gov/pubmed/32395410
http://dx.doi.org/10.1002/jmd2.12099

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