Germline intergenic duplications at Xq26.1 underlie Bazex–Dupré–Christol basal cell carcinoma susceptibility syndrome *
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DOI: 10.1111/bjd.21842
Abstract: Bazex–Dupré–Christol syndrome (BDCS; MIM301845) is a rare X‐linked dominant genodermatosis characterized by follicular atrophoderma, congenital hypotrichosis and multiple basal cell carcinomas (BCCs). Previous studies have linked BDCS to an 11·4‐Mb interval on chromosome Xq25‐q27.1. However,… read more here.
Keywords: basal cell; dupr christol; bazex dupr;
Bazex‐Dupré‐Christol syndrome: review of clinical and molecular aspects
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DOI: 10.1111/ijd.14065
Abstract: Bazex‐Dupré‐Christol syndrome is a rare genodermatosis that manifests with the classical triad of basal cell carcinoma, follicular atrophoderma, and hypotrichosis; yet it may be accompanied by milia, ichthyosis, neurological symptoms, and visceral malignancies. Symptom onset… read more here.
Keywords: molecular aspects; review clinical; bazex dupr; christol syndrome ... See more keywords