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People with polymerase eta pathogenic variants have the same cutaneous and ocular findings as other XP patients but do not have progressive neurologic degeneration.[65] A founder pathogenic variant resulting in a deletion of exon 10 was seen in 16 of 16 individuals from ten Tunisian consanguineous families.[66] Work on genotype-phenotype correlations among the XP complementation groups continues

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Moreover, the field of eryptosis research focuses primarily on the preclinical in vitro evaluation of compounds that might theoretically induce eryptosis

Always consult with your doctor if you intend to delay your period but still wish to conceive