Tooth and nail syndrome: Difference between revisions
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Created page with "{{Infobox_Disease | OMIM = 189500 | ICD10 ={{ICD10|Q|82|4|q|82}}| }} '''Tooth and nail syndrome''' (also known as "Hypodontia with nail dysgenesis,"<ref name="Fitz..." |
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ICD10 ={{ICD10|Q|82|4|q|82}}| | ICD10 ={{ICD10|Q|82|4|q|82}}| | ||
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==Overview== | |||
'''Tooth and nail syndrome''' (also known as "Hypodontia with nail dysgenesis,"<ref name="Fitz2" /> and "Witkop syndrome"<ref name="Fitz2" />) is a rare disorder, first described in 1965, characterized by nails that are thin, small, and friable, and which may show koilonychia at birth.<ref name="Fitz2">Freedberg, et al. (2003). ''Fitzpatrick's Dermatology in General Medicine''. (6th ed.). McGraw-Hill. ISBN 0-07-138076-0.</ref>{{rp|521}}<ref name="Bolognia">{{cite book |author=Rapini, Ronald P.; Bolognia, Jean L.; Jorizzo, Joseph L. |title=Dermatology: 2-Volume Set |publisher=Mosby |location=St. Louis |year=2007 |pages=880 |isbn=1-4160-2999-0 |oclc= |doi= |accessdate=}}</ref> | '''Tooth and nail syndrome''' (also known as "Hypodontia with nail dysgenesis,"<ref name="Fitz2" /> and "Witkop syndrome"<ref name="Fitz2" />) is a rare disorder, first described in 1965, characterized by nails that are thin, small, and friable, and which may show koilonychia at birth.<ref name="Fitz2">Freedberg, et al. (2003). ''Fitzpatrick's Dermatology in General Medicine''. (6th ed.). McGraw-Hill. ISBN 0-07-138076-0.</ref>{{rp|521}}<ref name="Bolognia">{{cite book |author=Rapini, Ronald P.; Bolognia, Jean L.; Jorizzo, Joseph L. |title=Dermatology: 2-Volume Set |publisher=Mosby |location=St. Louis |year=2007 |pages=880 |isbn=1-4160-2999-0 |oclc= |doi= |accessdate=}}</ref> | ||
Revision as of 20:07, 31 July 2012
| Tooth and nail syndrome | |
| ICD-10 | Q82.4 |
|---|---|
| OMIM | 189500 |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Overview
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
References
- ↑ 1.0 1.1 1.2 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 1-4160-2999-0.
- ↑ Jumlongras D, Bei M, Stimson JM; et al. (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. Unknown parameter
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