Gingival Fibromatosis with Hypertrichosis Latest Advances

Generalised Gingival Fibromatosis and Hypertrichosis: A Rare Case of Syndromic Presentation.

Journal: Cureus

Published: January 07, 2026

Absence of Neurodevelopmental Impairment in an Individual With KCNN3 -Related Zimmermann Laband Syndrome.

Journal: American journal of medical genetics. Part A

Published: August 14, 2024

Clinical management of hereditary gingival fibromatosis: Case report with 13 years follow-up.

Journal: Clinical advances in periodontics

Published: August 09, 2024

Genetic Variants in the TBC1D2B Gene Are Associated with Ramon Syndrome and Hereditary Gingival Fibromatosis.

Journal: International journal of molecular sciences

Published: June 20, 2024

ELMO2 biallelic pathogenic variants in a patient with gingival hypertrophy and cherubism phenotype: Case report and molecular review.

Journal: American journal of medical genetics. Part A

Published: January 27, 2024

A recurrent KCNK4 variant in a dominant pedigree with hypertrichosis and gingival fibromatosis syndrome: Variable phenotypic expressivity and insights on patients' dental management.

Journal: American journal of medical genetics. Part A

Published: May 10, 2023

Zimmermann-Laband syndrome-associated hereditary gingival fibromatosis.

Journal: Journal of Indian Society of Periodontology

Published: December 21, 2022

Genetic architecture and phenotypic landscape of deafness and onychodystrophy syndromes.

Journal: Human genetics

Published: May 07, 2021

Zimmermann-Laband syndrome in monozygotic twins with a mild neurobehavioral phenotype lacking gingival overgrowth-A case report of a novel KCNN3 gene variant.

Journal: American journal of medical genetics. Part A

Published: March 15, 2021

Syndromic disorders caused by gain-of-function variants in KCNH1, KCNK4, and KCNN3-a subgroup of K+ channelopathies.

Journal: European journal of human genetics : EJHG

Published: November 09, 2020

Patients with KCNH1-related intellectual disability without distinctive features of Zimmermann-Laband/Temple-Baraitser syndrome.

Journal: Journal of medical genetics

Published: October 14, 2020

"Electrifying dysmorphology": Potassium channelopathies causing dysmorphic syndromes.

Journal: Advances in genetics

Published: June 21, 2020

Gingival Fibromatosis with Hypertrichosis Latest Advances

Find the Latest Research About Gingival Fibromatosis with Hypertrichosis

Generalised Gingival Fibromatosis and Hypertrichosis: A Rare Case of Syndromic Presentation.

Generalised Gingival Fibromatosis and Hypertrichosis: A Rare Case of Syndromic Presentation.

Absence of Neurodevelopmental Impairment in an Individual With KCNN3 -Related Zimmermann Laband Syndrome.

Absence of Neurodevelopmental Impairment in an Individual With KCNN3 -Related Zimmermann Laband Syndrome.

Clinical management of hereditary gingival fibromatosis: Case report with 13 years follow-up.

Clinical management of hereditary gingival fibromatosis: Case report with 13 years follow-up.

Genetic Variants in the TBC1D2B Gene Are Associated with Ramon Syndrome and Hereditary Gingival Fibromatosis.

Genetic Variants in the TBC1D2B Gene Are Associated with Ramon Syndrome and Hereditary Gingival Fibromatosis.

ELMO2 biallelic pathogenic variants in a patient with gingival hypertrophy and cherubism phenotype: Case report and molecular review.

ELMO2 biallelic pathogenic variants in a patient with gingival hypertrophy and cherubism phenotype: Case report and molecular review.

A recurrent KCNK4 variant in a dominant pedigree with hypertrichosis and gingival fibromatosis syndrome: Variable phenotypic expressivity and insights on patients' dental management.

A recurrent KCNK4 variant in a dominant pedigree with hypertrichosis and gingival fibromatosis syndrome: Variable phenotypic expressivity and insights on patients' dental management.

Zimmermann-Laband syndrome-associated hereditary gingival fibromatosis.

Zimmermann-Laband syndrome-associated hereditary gingival fibromatosis.

Genetic architecture and phenotypic landscape of deafness and onychodystrophy syndromes.

Genetic architecture and phenotypic landscape of deafness and onychodystrophy syndromes.

Zimmermann-Laband syndrome in monozygotic twins with a mild neurobehavioral phenotype lacking gingival overgrowth-A case report of a novel KCNN3 gene variant.

Zimmermann-Laband syndrome in monozygotic twins with a mild neurobehavioral phenotype lacking gingival overgrowth-A case report of a novel KCNN3 gene variant.

Syndromic disorders caused by gain-of-function variants in KCNH1, KCNK4, and KCNN3-a subgroup of K+ channelopathies.

Syndromic disorders caused by gain-of-function variants in KCNH1, KCNK4, and KCNN3-a subgroup of K+ channelopathies.

Patients with KCNH1-related intellectual disability without distinctive features of Zimmermann-Laband/Temple-Baraitser syndrome.

Patients with KCNH1-related intellectual disability without distinctive features of Zimmermann-Laband/Temple-Baraitser syndrome.

"Electrifying dysmorphology": Potassium channelopathies causing dysmorphic syndromes.

"Electrifying dysmorphology": Potassium channelopathies causing dysmorphic syndromes.