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Variable skin findings in two siblings with KDSR mutations manifesting in PERIOPTER syndrome
Daphne Wijsmans1, Ifigenia Spanoudi-Kitrimi1
1Department of Dermatology, University Hospital Leuven, Leuven, Belgium.
Abstract:
Pathogenic variants in the KDSR gene give rise to a Mendelian disorder called PERIOPTER syndrome. The disease is caused by a disruption in ceramide synthesis, with an impact on both skin and bone marrow. Patients with PERIOPTER syndrome show intermittent thrombocytopenia and/or associated anemia as well as disorders of keratinization. We present two siblings with identical compound heterozygous pathogenic variants in the KDSR gene, but with different clinical manifestations.
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