Sjogren‐Larsson syndrome associated hypermelanosis
YC Xu, JQ Hou, WJ Zhu, P Li - Journal of Cosmetic …, 2020 - Wiley Online Library
Abstract Background/Objectives Sjogren–Larsson syndrome (SLS) is a rare autosomal
recessive disease of the mutation ALDH 3A2 that identifies a part of fatty acids for fatty …
recessive disease of the mutation ALDH 3A2 that identifies a part of fatty acids for fatty …
[HTML][HTML] Sjögren-Larsson Syndrome: A Rare Presentation With Developmental Delay
KJ Srilakshmi, MD Waheed, S Batool, SS Holder… - Cureus, 2023 - ncbi.nlm.nih.gov
Sjögren-Larsson syndrome (SLS) is a rare, inherited disorder passed down through families
in an autosomal recessive pattern. Its main characteristics are spastic diplegic paralysis …
in an autosomal recessive pattern. Its main characteristics are spastic diplegic paralysis …
Sjogren–Larsson Syndrome: A case series of five members from an extended family with a novel mutation
Abstract Backgroundd Sjogren–Larsson syndrome (SLS) is a rare autosomal recessive
disorder, characterized by a triad of spastic tetraplegia or diplegia, congenital ichthyosis …
disorder, characterized by a triad of spastic tetraplegia or diplegia, congenital ichthyosis …
Dermatologic Manifestations of Neurologic Disease
Ü Türsen, B Türsen - Journal of the Turkish Academy of …, 2013 - search.proquest.com
Background: Many diseases present with both neurologic and dermatologic manifestations.
Eight such clinical cases are presented, along with clinical photographs of the skin lesions …
Eight such clinical cases are presented, along with clinical photographs of the skin lesions …
Sjogren–Larsson Syndrome: A Rare Case Report
V Shah, K Rambhia, J Mukhi… - Indian Dermatology …, 2018 - journals.lww.com
SLS is caused by a recessive mutation of the fatty aldehyde dehydrogenase (FALDH) gene
located on the short arm of chromosome 17 (17p11. 2), which leads to a deficiency of the …
located on the short arm of chromosome 17 (17p11. 2), which leads to a deficiency of the …
[引用][C] Expanding the Genotype of Sjögren-Larsson Syndrome: A New Case Due to Two Novel Mutations.
E García-Peris, I Latour-Álvarez… - Actas Dermo …, 2017 - europepmc.org
Expanding the Genotype of Sjögren-Larsson Syndrome: A New Case Due to Two Novel
Mutations. - Abstract - Europe PMC Sign in | Create an account https://orcid.org Europe PMC …
Mutations. - Abstract - Europe PMC Sign in | Create an account https://orcid.org Europe PMC …