Neurological Manifestations of X-Linked Ichthyosis: Case Report and Review of the Literature

<div>(a) Affymetrix CytoScan chromosomal microarray analysis detected a 1.7 Mb deletion at Xp22.31 (6,458,939–8,135,644, genome build hg 19) in our male patient. (b) UCSC genome browser image showing the Xp22.31 deletion. The deleted interval contains six known genes (PUDP, STS, MIR4767, VCX, PNPLA4, and MIR651).</div>

Case Reports in Genetics

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Figure 2

Figure 2: Neurological Manifestations of X-Linked Ichthyosis: Case Report and Review of the Literature 