Progressive symmetrical erythrokeratoderma manifesting as harlequin-like ichthyosis with severe thrombocytopenia secondary to a homozygous 3-ketodihydrosphingosine reductase mutation

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Cyhoeddwyd yn:JAAD Case Rep
Prif Awduron: Altawil, Lama, Alshihry, Hind, Alfaraidi, Huda, Alhashem, Amal, Alhumidi, Ahmed, Alkuraya, Fowzan S.
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: Elsevier 2021
Pynciau:
Case Report
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC8261470/
https://ncbi.nlm.nih.gov/pubmed/34277909
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.jdcr.2021.06.006
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