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Genetic and developmental disorders of the oral mucosa: Epidemiology; molecular mechanisms; diagnostic criteria; management

Authors: Pinna; Roberto; Cocco; Fabio; Campus; Guglielmo; CONTI G; +6 Authors

Genetic and developmental disorders of the oral mucosa: Epidemiology; molecular mechanisms; diagnostic criteria; management

Abstract

AbstractA large number of disorders may affect the oral cavity, including genetic diseases, infections, cancers, blood diseases, skin diseases, endocrine and metabolic disorders, autoimmune and rheumatologic diseases, local lesions, to name a few. Oral mucosa shows a considerable variation in its normal structure and a wide range of conditions may affect it. Such conditions are often harmless or minor and could be primary or secondary to systemic disease. Several of them are quite rare and, hence, the diagnosis is not easy. Clinically, lesions may appear as ulcers, discoloration of the oral mucosa and alterations in size and configuration of oral anatomy. Genetic disorders have specific manifestations and can be caused by a derangement of one or more components of the tissue. Many of them follow the skin or systemic signs of the underlying genetic disease, but in a few cases oral signs could be the first manifestation of the disorder. Among them genodermatoses are prominent. They are inherited disorders characterized by a multisystem involvement. This review describes chondro‐ectodermal dysplasia, dyskeratosis congenita, Ehlers‐Danlos syndrome, hereditary benign intraepithelial dyskeratosis, keratosis follicularis, lipoid proteinosis, multiple hamartoma syndrome, pachyonychia congenita, Peutz‐Jeghers syndrome, tuberous sclerosis and white sponge nevus. Other genetic disorders not included in the genodermatosis group and reported in the present review are: acanthosis nigricans, angio‐osteo‐hypertrophic syndrome, encephalotrigeminal angiomatosis, familial adenomatous polyposis, focal dermal hypoplasia, focal palmoplantar and oral mucosa hyperkeratosis syndrome, gingival fibromatosis, Maffucci's syndrome, neurofibromatosis (type 1) and oro‐facial‐digital syndrome (type 1). Disorders during embryonic development might lead to a wide range of abnormalities in the oral cavity; some of them are quite common but of negligible concern, whereas others are rare but serious, affecting not only the oral mucosa, but also other structures of the oral cavity (ie palate, tongue and gingiva). Fordyce′s granules, leukoedema, cysts of the oral mucosa in newborns, retrocuspid papilla, geographic tongue, fissured tongue, median rhomboid glossitis, hairy tongue, lingual varices and lingual thyroid nodule are described. This review may help dentists, dental hygienists, but also general internists and pediatricians to diagnose different disorders of the oral mucosa, to understand the pathogenesis and to schedule a treatment plan.

Country
Italy
Keywords

oral mucosa, genetic developmental, oral genetic diseases, oral developmental diseases, oral mucosal diseases, chondro-ectodermal dysplasia, dyskeratosis congenita, Ehlers-Danlos syndrome, hereditary benign intraepithelial dyskeratosis, keratosis follicularis, lipoid proteinosis, Multiple hamartoma syndrome, Pachyonychia congenita, Peutz-Jeghers syndrome, Tuberous sclerosis, white sponge nevus, acanthosis nigricans, angio-osteo-hypertrophic syndrome, encephalotrigeminal angiomatosis Familial adenomatous polyposis, focal dermal hypoplasia, focal palmoplantar syndrome, gingival fibromatosis, Maffucci’s syndrome, neurofibromatosis, oro-facial-digital syndrome, Epstein's pearls, Fordyce′s granules, leukoedema, retrocuspid papilla, geographic tongue, fissured tongue, median rhomboid glossitis, hairy tongue, lingual varices, lingual thyroid nodule, Infant, Newborn, Mouth Mucosa, Periodontics, Humans, epidemiology, oral genetic diseases; oral developmental diseases; oral mucosal diseases; chondro-ectodermal dysplasia; dyskeratosis congenita; Ehlers-Danlos syndrome; hereditary benign intraepithelial dyskeratosis; keratosis follicularis; lipoid proteinosis; Multiple hamartoma syndrome; Pachyonychia congenita; Peutz-Jeghers syndrome; Tuberous sclerosis; white sponge nevus; acanthosis nigricans; angio-osteo-hypertrophic syndrome; encephalotrigeminal angiomatosis Familial adenomatous polyposis; focal dermal hypoplasia; focal palmoplantar syndrome; gingival fibromatosis; Maffucci’s syndrome; neurofibromatosis; oro-facial-digital syndrome; Epstein's pearls; Fordyce′s granules; leukoedema; retrocuspid papilla; geographic tongue; fissured tongue; median rhomboid glossitis; hairy tongue; lingual varices; lingual thyroid nodule, Mouth Diseases

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    popularity
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    influence
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    impulse
    This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
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selected citations
These citations are derived from selected sources.
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
46
Top 10%
Top 10%
Top 10%
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