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
Researcher Affiliations
- Human Medical Genetics Program and Department of Pediatrics, University of Colorado Health Sciences Center, Denver, Colorado 80262, USA. richard.spitz@uchsc.edu
MeSH Terms
- Animals
- History, 20th Century
- Humans
- Neurofibromatosis 1 / history
- Piebaldism / history
Citations
This article has been cited 4 times.- 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.
- 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.
- 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.
- 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.
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