ORCID ID
Yasemin Yavuz : https://orcid.org/0000-0001-5961-4996
Mehmet Sinan Doğan : https://orcid.org/0000-0002-3089-1305
Myroslav Goncharuk-Khomyn : https://orcid.org/0000-0002-7482-3881
Abstract
Background: Ectodermal dysplasia is a complex group of genetic disorders identified through the abnormal development of ectodermal structures. It is a genetic disorder that affects the development or functions of tissues such as the teeth, hair, nails, and sweat glands.
Methods: This review aimed to introduce the outcomes and increase awareness of ectodermal dysplasia reviewing by the literature.
Results: The characteristic features of this disease, including hypodontia, hypohidrosis, and hypotrichosis, have been discussed.
Conclusions: Ectodermal dysplasia is a heterogeneous group of hereditary disorders with similar clinical findings. It leads to the development of tissue malformations and affects the quality of life of the patient. This review demonstrates that dentists can provide viable and safe alternative conventional treatment modalities for oral rehabilitation in patients with ectodermal dysplasia.
References
- Anbouba GM, Carmany EP, Natoli JL. The characterization of hypodontia, hypohidrosis, and hypotrichosis associated with X-linked hypohidrotic ectodermal dysplasia: A systematic review. Am J Med Genet A. 2020;182:831–41.
- Swathi G, Ramesh T, Sravani KB. Ectodermal dysplasia-a report of two cases. Indian J Clin Dent. 2020;1:10–3.
- Itin PH. Etiology and pathogenesis of ectodermal dysplasias. Am J Med Genet A. 2014;164A:2472–7
- Goncharuk-Khomyn M, Yavuz I, Cavalcanti A, Boykiv A, Nahirny Y. Key aspects of dental diagnostics and treatment specifics in ectodermal dysplasia patients: Comprehensive literature review. J Stomatol. 2020:73:342–50.
- Goker F, Grecchi E, Mancini EG, Del Fabbro M, Grecchi F. Zygomatic implant survival in 9 ectodermal dysplasia patients with 3.5- to 7-year follow-up. Oral Dis. 2020;26:1803–9.
- Callea M, Nieminen P, Willoughby CE, Clarich G, Yavuz I, Vinciguerra A, et al. A novel INDEL mutation in the EDA gene resulting in a distinct X- linked hypohidrotic ectodermal dysplasia phenotype in an Italian family. J Eur Acad Dermatol Venereol. 2016;30:341–3.
- Yavuz I, Baskan Z, Ulku R, Dulgergil TC, Dari O, Ece A, et al. Ectodermal dysplasia: Retrospective study of fifteen cases. Arch Med Res. 2006;37:403–9.
- Lamartine J. Towards a new classification of ectodermal dysplasias. Clin Exp Dermatol. 2003;28:351–5.
- Itin PH. Ectodermal dysplasia: thoughts and practical concepts concerning disease classification - The role of functional pathways in the molecular genetic diagnosis. Dermatol. 2013;226:111–4.
- Deshmukh S, Prashanth S. Ectodermal dysplasia: a genetic review. Int J Clin Pediatr Dent. 2012;5:197–202.
- Priolo M, Laganà C. Ectodermal dysplasias: a new clinical-genetic classification. J Med Genet. 2001;38:579–85.
- Wright JT, Fete M, Schneider H, Zinser M, Koster MI, Clarke AJ, et al. Ectodermal dysplasias: Classification and organization by phenotype, genotype and molecular pathway. Am J Med Genet A. 2019;179:442–7.
- The Ectodermal Dysplasia Society. Alphabetical List of Types of ED. United Kingdom: The Ectodermal Dysplasia Society, 2021.
- Kearns G, Sharma A, Perrott D, Schmidt B, Kaban L, Vargervik K. Placement of endosseous implants in children and adolescents with hereditary ectodermal dysplasia. Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 1999l;88:5–10.
- Guckes AD, McCarthy GR, Brahim J. Use of endosseous implants in a 3-year-old child with ectodermal dysplasia: case report and 5-year follow-up. Pediatr Dent. 1997;19:282–5.
- Percinoto C, Vieira AE, Barbieri CM, Melhado FL, Moreira KS. Use of dental implants in children: a literature review. Quintessence Int. 2001;32:381–3.
- Meza Escobar LE, Isaza C, Pachajoa H. Síndrome de ectrodactilia, displasia ectodérmica y fisura de labio/paladar, informe de un caso con expresividad variable [Ectrodactyly, ectodermal dysplasia and cleft lip/palate syndrome, report of a case with variable expressivity]. Arch Argent Pediatr. 2012;110:e95–8.
- García-Martín P,Hernández-Martín A, Torrelo A. Displasias ectodérmicas: Revisión clínica y molecular [Ectodermal dysplasias: A clinical and molecular review]. Actas Dermosifiliogr. 2013;104:451–70.
- Priolo M. Ectodermal dysplasias: An overview and update of clinical and molecular-functional mechanisms. Am J Med Genet A. 2009;149A:2003–13.
- Yin W, Ye X, Bian Z. The second deletion mutation in exon 8 of EDA gene in an XLHED pedigree. Dermatol. 2013;226:105–10.
- Panda SP. Ectodermal dysplasia: An overview. Indian J Forensic Med Toxicol. 2020;14:9071–4.
- Huttner K. Future developments in XLHED treatment approaches. Am J Med Genet A. 2014;164A:2433–6.
Recommended Citation
Yavuz Y, Doğan MS, Goncharuk-Khomyn M. Ectodermal Dysplasia: A Review. Makara J Health Res. 2021;25.
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