Hand-Foot-Genital Syndrome Latest Advances

Find the Latest Research About Hand-Foot-Genital Syndrome

Last Updated: 02/24/2026

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Found 12 publications

Hand-foot-genital syndrome due to a duplication variant in the GC-rich region of HOXA13.

Hand-foot-genital syndrome due to a duplication variant in the GC-rich region of HOXA13.

Journal: European journal of medical genetics
Published: July 14, 2022

"Hand foot genital syndrome": Proposition of a new term, induced by Sunitinib in a patient of metastatic renal cell carcinoma.

"Hand foot genital syndrome": Proposition of a new term, induced by Sunitinib in a patient of metastatic renal cell carcinoma.

Journal: Dermatologic therapy
Published: November 10, 2020

50 Years Ago in The Journal of Pediatrics: Hand-Foot-Genital Syndrome and Its Multiple Genetic Mechanisms.

50 Years Ago in The Journal of Pediatrics: Hand-Foot-Genital Syndrome and Its Multiple Genetic Mechanisms.

Journal: The Journal of pediatrics
Published: June 27, 2020

Multifaceted Hoxa13 function in urogenital development underlies the Hand-Foot-Genital Syndrome.

Multifaceted Hoxa13 function in urogenital development underlies the Hand-Foot-Genital Syndrome.

Journal: Human molecular genetics
Published: October 15, 2018

Hand-foot-genital syndrome - analysis of two cases.

Hand-foot-genital syndrome - analysis of two cases.

Journal: JBRA assisted reproduction
Published: April 12, 2018

A missense mutation of HOXA13 underlies hand-foot-genital syndrome in a Chinese family.

A missense mutation of HOXA13 underlies hand-foot-genital syndrome in a Chinese family.

Journal: Journal of genetics
Published: September 27, 2017

Familial deletion of the HOXA gene cluster associated with Hand-Foot-Genital syndrome and phenotypic variability.

Familial deletion of the HOXA gene cluster associated with Hand-Foot-Genital syndrome and phenotypic variability.

Journal: American journal of medical genetics. Part A
Published: May 20, 2016

A Chromosome 7 Pericentric Inversion Defined at Single-Nucleotide Resolution Using Diagnostic Whole Genome Sequencing in a Patient with Hand-Foot-Genital Syndrome.

A Chromosome 7 Pericentric Inversion Defined at Single-Nucleotide Resolution Using Diagnostic Whole Genome Sequencing in a Patient with Hand-Foot-Genital Syndrome.

Journal: PloS one
Published: March 24, 2016

Dual genetic diagnoses: Atypical hand-foot-genital syndrome and developmental delay due to de novo mutations in HOXA13 and NRXN1.

Dual genetic diagnoses: Atypical hand-foot-genital syndrome and developmental delay due to de novo mutations in HOXA13 and NRXN1.

Journal: American journal of medical genetics. Part A
Published: February 08, 2015

Severe manifestations of hand-foot-genital syndrome associated with a novel HOXA13 mutation.

Severe manifestations of hand-foot-genital syndrome associated with a novel HOXA13 mutation.

Journal: American journal of medical genetics. Part A
Published: September 02, 2013

Analysis of de novo HOXA13 polyalanine expansions supports replication slippage without repair in their generation.

Analysis of de novo HOXA13 polyalanine expansions supports replication slippage without repair in their generation.

Journal: American journal of medical genetics. Part A
Published: October 03, 2012

Hand-foot-genital syndrome with a 7p15 deletion: clinically recognizable syndrome.

Hand-foot-genital syndrome with a 7p15 deletion: clinically recognizable syndrome.

Journal: Pediatrics international : official journal of the Japan Pediatric Society
Published: May 29, 2012
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Last Updated: 02/24/2026