Results 51 to 60 of about 1,146 (168)

Ambras syndrome: A rare case report

open access: yesJournal of Indian Society of Pedodontics and Preventive Dentistry, 2016
Congenital generalized hypertrichosis associated with gingival hyperplasia are rare cases published in literature. The frequency incidence of generalized congenital hypertrichosis is about one to billions of people.
A Ishita   +3 more
doaj   +1 more source

Nifedipine Induces FAM20A Upregulation and LRP2/CUBN‐Mediated Fetuin‐A Accumulation in Gingival Overgrowth

open access: yesInternational Journal of Dentistry, Volume 2026, Issue 1, 2026.
Aim Nifedipine‐induced gingival overgrowth (NIGO) has been linked to fibrotic remodeling of the gingiva, yet whether FAM20A and Fetuin‐A contribute to this process is unknown. Here we ask whether their expression is altered in NIGO and, if so, whether nifedipine itself drives this change.
Isaac De la Rosa   +9 more
wiley   +1 more source

Fibromatosis gingival hereditaria

open access: yes, 2020
Fil: Faur, María Sol. Hospital Central de Mendoza (Argentina)
Faur, María Sol   +4 more
openaire   +3 more sources

Early Recognition of Infantile Systemic Hyalinosis in a Palestinian Infant: A Case Report

open access: yesClinical Case Reports, Volume 13, Issue 10, October 2025.
ABSTRACT Infantile systemic hyalinosis should be suspected in infants with contractures, skin changes, and diarrhea in consanguineous families. Early recognition allows timely genetic testing, supportive care, and counseling, improving family outcomes despite poor prognosis.
Lilyan Jarrar   +6 more
wiley   +1 more source

Surgical Management of Severe Drug‐Induced Gingival Hypertrophy: A Case Report

open access: yesClinical Case Reports, Volume 13, Issue 10, October 2025.
Hyperplastic changes of the maxillary and mandibular gingiva with pedunculated lesion along the right mandible. ABSTRACT Gingival enlargement is an adverse effect of certain medications, most notably calcium channel blockers, immunosuppressants, and anticonvulsants.
John J. Alfarone   +3 more
wiley   +1 more source

Non syndromic gingival fibromatosis in a mild mental retardation child

open access: yesContemporary Clinical Dentistry, 2012
Gingival fibromatosis is a benign oral condition characterized by enlargement of gingival tissues. It usually develops as an isolated disorder but can be one of the features of a syndrome.
Mahesh K Duddu   +3 more
doaj   +1 more source

Gingival enlargement following levetiracetam treatment: A clinical case analysis

open access: yesEpilepsia Open, Volume 10, Issue 5, Page 1695-1698, October 2025.
Abstract This report describes a 21‐year‐old female with a history of epilepsy, diagnosed at age 17, who developed gingival enlargement after being treated with levetiracetam. Her dosage was titrated to 750 mg twice daily, achieving satisfactory seizure control.
Awadh M. Alahmari, Ali M. Alkhathaami
wiley   +1 more source

The Autosomal Recessive Inheritance of Hereditary Gingival Fibromatosis

open access: yesCase Reports in Dentistry, 2013
Hereditary gingival fibromatosis (HGF) is a rare condition which is marked by enlargement of gingival tissue that covers teeth to various extents leading to aesthetic disfigurement.
Poulami Majumder   +4 more
doaj   +1 more source

A case of gingival fibromatosis.

open access: yesJapanese Journal of Oral & Maxillofacial Surgery, 1988
A case of gingival fibromatosis in a 15-year-old male is reported. This disease israre and its etiology is unknown. The symptoms of gingival fibromatosis show diffuse, extensive and hyperplastic gingiva, and not much inflammatory change. It was suspected that the causes of this case were related to the developmental anomalies and eruption stimuli. Only
KOTSUGAI, Takeshi   +4 more
openaire   +2 more sources

Genetic Insights Into Hyaline Fibromatosis Syndrome: A Case Report of an ANTXR2 Mutation Featuring a Rare Variant c.697+1G>A

open access: yesClinical Case Reports, Volume 13, Issue 4, April 2025.
ABSTRACT Hyaline fibromatosis syndrome (HFS) is a rare genetic disorder encompassing juvenile hyaline fibromatosis (JHF) and infantile systemic hyalinosis (ISH), caused by mutations in the anthrax toxin receptor 2 gene (ANTXR2). This condition leads to the accumulation of hyaline plaques in the skin and organs, resulting in symptoms such as skin ...
Shabnam Hajiani Ghotbabadi   +3 more
wiley   +1 more source

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