Health Conditions Related to Genetic Changes
Nonsyndromic congenital nail disorder 10
At least three mutations in the FZD6 gene have been found to cause nonsyndromic congenital nail disorder 10. This condition is characterized by abnormally thick fingernails and toenails that may appear claw-like. The mutations lead to the production of a frizzled-6 protein that cannot get to the cell membrane where it is needed or that cannot transmit signals into the cell. As a result, Wnt signaling is disrupted and the growth and development of nails is poorly regulated, which leads to separation of the nail from the underlying nail bed (onycholysis) and other abnormalities of the fingernails and toenails.
More About This Health ConditionOther Names for This Gene
- frizzled 6, seven transmembrane spanning receptor
- frizzled family receptor 6
- frizzled homolog 6
- FZ-6
- FZ6
- HFZ6
Additional Information & Resources
Tests Listed in the Genetic Testing Registry
Scientific Articles on PubMed
Catalog of Genes and Diseases from OMIM
References
- Frojmark AS, Schuster J, Sobol M, Entesarian M, Kilander MBC, Gabrikova D, Nawaz S, Baig SM, Schulte G, Klar J, Dahl N. Mutations in Frizzled 6 cause isolated autosomal-recessive nail dysplasia. Am J Hum Genet. 2011 Jun 10;88(6):852-860. doi: 10.1016/j.ajhg.2011.05.013. Citation on PubMed or Free article on PubMed Central
- Guo N, Hawkins C, Nathans J. Frizzled6 controls hair patterning in mice. Proc Natl Acad Sci U S A. 2004 Jun 22;101(25):9277-81. doi: 10.1073/pnas.0402802101. Epub 2004 May 28. Citation on PubMed or Free article on PubMed Central
- Naz G, Pasternack SM, Perrin C, Mattheisen M, Refke M, Khan S, Gul A, Simons M, Ahmad W, Betz RC. FZD6 encoding the Wnt receptor frizzled 6 is mutated in autosomal-recessive nail dysplasia. Br J Dermatol. 2012 May;166(5):1088-94. doi: 10.1111/j.1365-2133.2011.10800.x. Epub 2012 Apr 4. Citation on PubMed
- Raza SI, Muhammad N, Khan S, Ahmad W. A novel missense mutation in the gene FZD6 underlies autosomal recessive nail dysplasia. Br J Dermatol. 2013 Feb;168(2):422-5. doi: 10.1111/j.1365-2133.2012.11203.x. Epub 2012 Oct 5. Citation on PubMed
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