Inviting an author to review:
Find an author and click ‘Invite to review selected article’ near their name.
Search for authorsSearch for similar articles
36
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      Management of pedal fibrovascular papillomas in Goltz-Gorlin syndrome

      JAAD Case Reports
      Elsevier BV

      Read this article at

          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Related collections

          Most cited references8

          • Record: found
          • Abstract: found
          • Article: not found

          Mutations in X-linked PORCN, a putative regulator of Wnt signaling, cause focal dermal hypoplasia.

          Focal dermal hypoplasia is an X-linked dominant disorder characterized by patchy hypoplastic skin and digital, ocular and dental malformations. We used array comparative genomic hybridization to identify a 219-kb deletion in Xp11.23 in two affected females. We sequenced genes in this region and found heterozygous and mosaic mutations in PORCN in other affected females and males, respectively. PORCN encodes the human homolog of Drosophila melanogaster porcupine, an endoplasmic reticulum protein involved in secretion of Wnt proteins.
            Bookmark
            • Record: found
            • Abstract: not found
            • Article: not found

            Focal dermal hypoplasia.

              Bookmark
              • Record: found
              • Abstract: not found
              • Article: not found

              Focal dermal hypoplasia syndrome. An update.

              R GOLTZ (1992)
                Bookmark

                Author and article information

                Journal
                10.1016/j.jdcr.2016.07.001
                http://creativecommons.org/licenses/by-nc-nd/4.0/

                Comments

                Comment on this article