• A novel mutation in TRPV3 gene causes atypical familial Olmsted syndrome
• A Rare Syndrome Resembling Scleroderma: Huriez Syndrome
• An SRY-negative XX male with Huriez syndrome
• An unusual case of palmoplantar keratoderma
• Case report: squamous cell carcinoma, radial forearm flap and Huriez syndrome. Focus on a rare pathology
• Claude Huriez and his syndrome
• Clinical images: Huriez syndrome, a rare scleroderma mimic
• Huriez syndrome associated with basal cell carcinoma. A case report
• Huriez syndrome caused by a large deletion that abrogates the skin-specific isoform of SMARCAD1
• Huriez syndrome finally explained: Haploinsufficiency of a gene involved in homologous recombination DNA repair
• Huriez syndrome with squamous cell carcinoma
• Huriez syndrome: Additional pathogenic variants supporting allelism to SMARCAD syndrome
• Keratoderma with scleroatrophy of the extremities or sclerotylosis (Huriez syndrome): a reappraisal
• Sclero-atrophic keratodermal genodermatosis of the extremities (sclerotylosis) (author's transl)
• SMARCAD1 Haploinsufficiency Underlies Huriez Syndrome and Associated Skin Cancer Susceptibility
• Unusual exophytic inclusion warts as a cutaneous horn on the dorsum of the hand