# The Dental and Oral Significance of Hutchinson-Gilford Prfogeria Syndrome: The Dental and Oral Significance of Hutchinson-Gilford Prfogeria Syndrome

**Authors:** Safa Saeed, Jawaher Abdulaziz Alhababi, Fatimah Alanazi, Amal Albarrak, Halh Alabdulmonem, Alanoud Inad Alenazi, Maha Alsane, Myle Akshay Kiran

PMC · DOI: 10.31661/gmj.vi.3763 · 2025-01-20

## TL;DR

This paper reviews the dental and oral issues in Hutchinson-Gilford Progeria Syndrome, highlighting their importance for diagnosis and treatment.

## Contribution

The paper provides a comprehensive overview of oral manifestations in HGPS and emphasizes the need for multidisciplinary care.

## Key findings

- HGPS patients show dental issues like delayed eruption, microdontia, and tooth loss.
- A multidisciplinary approach is needed for managing HGPS-related oral complications.
- Advances in genetic research may lead to targeted therapies for HGPS dental problems.

## Abstract

Hutchinson-Gilford Progeria Syndrome (HGPS) is a rare genetic disorder caused by a point mutation in the LMNA gene that encodes lamin A. This mutation results in the production of progerin, a defective protein that accelerates cellular aging. This review explores the oral and dental manifestations of HGPS, emphasizing their role in early diagnosis, management strategies, and the potential for targeted therapies.

A thorough review of existing literature was conducted to summarize the phenotypic characteristics, oral health implications, and current approaches for the management of HGPS-related complications.

Individuals with HGPS exhibit age-associated complications starting in early childhood, including distinct craniofacial abnormalities and severe oral health challenges. Common oral manifestations include delayed tooth eruption, microdontia, malocclusion, dental caries, tooth loss, and mandibular osteolysis. These abnormalities necessitate a multidisciplinary approach involving pediatric dentists, orthodontists, oral surgeons, and geneticists to deliver comprehensive care.

Understanding the pathophysiological mechanisms behind HGPS oral anomalies is vital for improving diagnosis and treatment. Advances in genetic research hold promise for developing targeted interventions to alleviate dental complications and enhance the quality of life for affected individuals. Ongoing research and a collaborative care approach are essential to address the challenges posed by HGPS effectively.

## Linked entities

- **Genes:** LMNA (lamin A/C) [NCBI Gene 4000]
- **Proteins:** Lam (Lamin)
- **Diseases:** Hutchinson-Gilford Progeria Syndrome (MONDO:0008310), HGPS (MONDO:0008310)

## Full-text entities

- **Genes:** LMNA (lamin A/C) [NCBI Gene 4000] {aka CDCD1, CDDC, CMD1A, CMT2B1, EMD2, FPL}
- **Diseases:** dental caries (MESH:D003731), tooth eruption (MESH:D014079), tooth loss (MESH:D016388), microdontia (MESH:C538240), genetic disorder (MESH:D030342), mandibular osteolysis (MESH:D008338), HGPS (MESH:D011371), oral anomalies (MESH:C536272), malocclusion (MESH:D008310), craniofacial abnormalities (MESH:D019465)

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12169116/full.md

---
Source: https://tomesphere.com/paper/PMC12169116