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(Top)
 


1 See also  





2 References  





3 External links  














Tooth and nail syndrome






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From Wikipedia, the free encyclopedia
 


Tooth and nail syndrome
This condition is inherited in an autosomal dominant manner.
SpecialtyMedical genetics Edit this on Wikidata

Tooth and nail syndrome (also known as "Hypodontia with nail dysgenesis,"[1] and "Witkop syndrome"[1]) is a rare disorder, first described in 1965, characterized by nails that are thin, small, and friable, and which may show koilonychia at birth.[1]: 521 [2]

It is associated with MSX1.[3]

See also[edit]

References[edit]

  1. ^ a b c Freedberg, et al. (2003). Fitzpatrick's Dermatology in General Medicine. (6th ed.). McGraw-Hill. ISBN 0-07-138076-0.
  • ^ Rapini, Ronald P.; Bolognia, Jean L.; Jorizzo, Joseph L. (2007). Dermatology: 2-Volume Set. St. Louis: Mosby. p. 880. ISBN 978-1-4160-2999-1.
  • ^ Jumlongras D, Bei M, Stimson JM, et al. (July 2001). "A nonsense mutation in MSX1 causes Witkop syndrome". Am. J. Hum. Genet. 69 (1): 67–74. doi:10.1086/321271. PMC 1226049. PMID 11369996.
  • External links[edit]


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  • Retrieved from "https://en.wikipedia.org/w/index.php?title=Tooth_and_nail_syndrome&oldid=1222459473"

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    Syndromes
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