Related Experiment Video
Updated: Jul 18, 2026

Anterior High-Resolution Optical Coherence Tomography in the Diagnosis and Therapeutic Monitoring of Ocular Surface Squamous Neoplasia
Published on: August 9, 2024
Hereditary benign intraepithelial dyskeratosis: a new case?
Bruno Correia Jham1, Ricardo Alves Mesquita, Maria Cássia Ferreira Aguiar
1Department of Oral Surgery and Pathology, School of Dentistry, Federal University of Minas Gerais, Minas Gerais, Brazil.
Hereditary benign intraepithelial dyskeratosis (HBID), a rare disorder, is reported in a Brazilian patient, marking the first South American case. Family history suggests a genetic cause for this condition, typically seen in a specific North Carolina tribe.
Area of Science:
- Oral pathology
- Dermatology
- Genetics
Background:
- Hereditary benign intraepithelial dyskeratosis (HBID) is a rare genetic disorder.
- First described in 1960, most cases originate from a North Carolina Indigenous community.
Observation:
- A Brazilian patient presented with clinical and histological features consistent with HBID.
- The patient exhibited asymptomatic oral and ocular lesions.
Findings:
- This case represents the first documented instance of HBID in South America.
- The oral lesions were clinically similar to other conditions like white sponge nevus.
Implications:
- This finding expands the known geographical distribution of HBID.
- Further investigation into the genetic etiology of HBID in diverse populations is warranted.
Related Concept Videos
Clinical Applications of Epidermal Stem Cells
Renewal of Skin Epidermal Stem Cells
Desmosomes
Cellular Adaptation IV: Dysplasia and Metaplasia
Pedigree Analysis
Cells of the Epidermis
The cells in all these layers except the stratum basale are called keratinocytes, a type of cell that manufactures and stores the protein keratin. The keratinocytes in the stratum corneum are dead and regularly slough away, being replaced by cells from...

