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Page 1
Hand-Foot-Genital Syndrome.
Innis JW. Innis JW. 2006 Jul 11 [updated 2019 Aug 8]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. 2006 Jul 11 [updated 2019 Aug 8]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. PMID: 20301596 Free Books & Documents. Review.
CLINICAL CHARACTERISTICS: Hand-foot-genital syndrome (HFGS) is characterized by limb malformations and urogenital defects. ...Surveillance: Follow up with a urologist in the presence of vesicoureteral reflux and/or documented urinary tract infection. G …
CLINICAL CHARACTERISTICS: Hand-foot-genital syndrome (HFGS) is characterized by limb malformations and urogenita …
Hand-foot-genital syndrome due to a duplication variant in the GC-rich region of HOXA13.
Geng W, Li F, Zhang R, Cao L, Du X, Gu W, Xu M. Geng W, et al. Eur J Med Genet. 2023 Mar;66(3):104711. doi: 10.1016/j.ejmg.2023.104711. Epub 2023 Jan 24. Eur J Med Genet. 2023. PMID: 36702441
BACKGROUND: Hand-Foot-Genital Syndrome (HFGS) is an autosomal dominant disorder characterized by a broad phenotypic spectrum. ...
BACKGROUND: Hand-Foot-Genital Syndrome (HFGS) is an autosomal dominant disorder characterized by a broad phenoty …
Multifaceted Hoxa13 function in urogenital development underlies the Hand-Foot-Genital Syndrome.
Roux M, Bouchard M, Kmita M. Roux M, et al. Hum Mol Genet. 2019 May 15;28(10):1671-1681. doi: 10.1093/hmg/ddz013. Hum Mol Genet. 2019. PMID: 30649340
Hand-Foot-Genital syndrome is a rare condition caused by mutations in the HOXA13 gene and characterized by limb malformations and urogenital defects. ...Using a conditional inactivation strategy, we show that mouse fetuses lacking Hoxa13 function devel …
Hand-Foot-Genital syndrome is a rare condition caused by mutations in the HOXA13 gene and characterized by limb …
An unusual manifestation of Hand-Foot-Genital Syndrome: Embryonal Rhabdomyosarcoma - A case report.
Hamza A, Ghannam G, Danial YK, Fattal A, Ghabreau L, Omar G, Abdullah M. Hamza A, et al. Ann Med Surg (Lond). 2021 Jan 19;62:175-178. doi: 10.1016/j.amsu.2021.01.032. eCollection 2021 Feb. Ann Med Surg (Lond). 2021. PMID: 33520218 Free PMC article.
Hand-Foot-Genital Syndrome (HFGS) is a dominantly inherited condition and one of the rarest cases encountered in clinical practice. ...This report emphasizes the need for a high index of suspicion to establish early detection of Embryonal Rhabdomyosarc …
Hand-Foot-Genital Syndrome (HFGS) is a dominantly inherited condition and one of the rarest cases encountered in …
Severe manifestations of hand-foot-genital syndrome associated with a novel HOXA13 mutation.
Imagawa E, Kayserili H, Nishimura G, Nakashima M, Tsurusaki Y, Saitsu H, Ikegawa S, Matsumoto N, Miyake N. Imagawa E, et al. Am J Med Genet A. 2014 Sep;164A(9):2398-402. doi: 10.1002/ajmg.a.36648. Epub 2014 Jun 16. Am J Med Genet A. 2014. PMID: 24934387
Heterozygous HOXA13 mutations have been previously reported in hand-foot-genital syndrome and Guttmacher syndrome, which are variably associated with small nails, short distal and middle phalanges, short thumbs and halluces, but not absent nails. ...
Heterozygous HOXA13 mutations have been previously reported in hand-foot-genital syndrome and Guttmacher syndrom …
Hand-foot-genital syndrome - analysis of two cases.
Piazza MJ, Urbanetz AA. Piazza MJ, et al. JBRA Assist Reprod. 2018 Jun 1;22(2):157-159. doi: 10.5935/1518-0557.20180025. JBRA Assist Reprod. 2018. PMID: 29638102 Free PMC article.
A missense mutation of HOXA13 underlies hand-foot-genital syndrome in a Chinese family.
Cao L, Chen C, Leng Y, Yan L, Wang S, Zhang X, Luo Y. Cao L, et al. J Genet. 2017 Sep;96(4):647-652. doi: 10.1007/s12041-017-0810-y. J Genet. 2017. PMID: 28947713 Free article.
Hand-foot-genital syndrome (HFGS) is a rare autosomal dominant inherited syndrome characterized by limb malformations and urogenital defects. ...
Hand-foot-genital syndrome (HFGS) is a rare autosomal dominant inherited syndrome characterized by limb malforma …
Familial deletion of the HOXA gene cluster associated with Hand-Foot-Genital syndrome and phenotypic variability.
Tas E, Sebastian J, Madan-Khetarpal S, Sweet P, Yatsenko AN, Pollock N, Rajkovic A, Schneck FX, Yatsenko SA, Witchel SF. Tas E, et al. Am J Med Genet A. 2017 Jan;173(1):221-224. doi: 10.1002/ajmg.a.37981. Epub 2016 Sep 20. Am J Med Genet A. 2017. PMID: 27649277
Hand-Foot-Genital syndrome is a rare autosomal dominant condition characterized by distal limb anomalies and urogenital malformations. ...This family was found to have the smallest reported deletion of 7p15.2 to date, and presented with features typica …
Hand-Foot-Genital syndrome is a rare autosomal dominant condition characterized by distal limb anomalies and uro …
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