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The Journal of investigative dermatology2004; 122(2); xxxiv-xxxv; doi: 10.1046/j.0022-202X.2004.22235.x

Piebaldism and neurofibromatosis type 1: horses of very different colors.

Abstract: No abstract available
Publication Date: 2004-03-11 PubMed ID: 15009761DOI: 10.1046/j.0022-202X.2004.22235.xGoogle Scholar: Lookup
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  • Historical Article
  • Journal Article

Cite This Article

APA
Spritz RA, Itin PH, Gutmann DH. (2004). Piebaldism and neurofibromatosis type 1: horses of very different colors. J Invest Dermatol, 122(2), xxxiv-xxxv. https://doi.org/10.1046/j.0022-202X.2004.22235.x

Publication

ISSN: 0022-202X
NlmUniqueID: 0426720
Country: United States
Language: English
Volume: 122
Issue: 2
Pages: xxxiv-xxxv

Researcher Affiliations

Spritz, Richard A
  • Human Medical Genetics Program and Department of Pediatrics, University of Colorado Health Sciences Center, Denver, Colorado 80262, USA. richard.spitz@uchsc.edu
Itin, Peter H
    Gutmann, David H

      MeSH Terms

      • Animals
      • History, 20th Century
      • Humans
      • Neurofibromatosis 1 / history
      • Piebaldism / history

      Citations

      This article has been cited 4 times.
      1. Wang C, Zhang Y, Hu X, Wang L, Xu Z, Xing H. Novel pathogenic variants in KIT gene in three Chinese piebaldism patients. Front Med (Lausanne) 2022;9:1040747.
        doi: 10.3389/fmed.2022.1040747pubmed: 36438053google scholar: lookup
      2. Akarsu S, İlknur T, Avcı C, Fetil E. Piebaldism Associated with Café-au-lait Macules and Intertriginous Freckling: A Case Report and Review of the Literature. Ann Dermatol 2019 Oct;31(5):567-570.
        doi: 10.5021/ad.2019.31.5.567pubmed: 33911651google scholar: lookup
      3. Zhang J, Li M, Yao Z. Molecular screening strategies for NF1-like syndromes with café-au-lait macules (Review). Mol Med Rep 2016 Nov;14(5):4023-4029.
        doi: 10.3892/mmr.2016.5760pubmed: 27666661google scholar: lookup
      4. Chiu YE, Dugan S, Basel D, Siegel DH. Association of Piebaldism, multiple café-au-lait macules, and intertriginous freckling: clinical evidence of a common pathway between KIT and sprouty-related, ena/vasodilator-stimulated phosphoprotein homology-1 domain containing protein 1 (SPRED1). Pediatr Dermatol 2013 May-Jun;30(3):379-82.