Long‐term dental management of a patient with features of Schöpf–Schulz–Passarge syndrome

Manchanda, Nandika; Anthonappa, Robert P.; Al-Mulla, Hessa; King, Nigel M.

doi:10.1111/scd.12228

Cited by 2 publications

(1 citation statement)

References 26 publications

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“…Over‐activation leads to misshapen and ectopic teeth, while under‐activation results in an arrest in tooth development (Liu et al, ). Schöpf–Schulz–Passarge is due to mutations in the Wnt10A gene and is characterized by hypodontia, palmoplantar keratoderma, and eyelid hidrocystomas among other features (Table ; Manchanda, Anthonappa, Al‐Mulla, & King, ).…”

Section: Molecular Pathways In Tooth Developmentmentioning

confidence: 99%

Genodermatoses with teeth abnormalities

et al. 2020

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Many genodermatoses exhibit abnormal teeth findings. Studies examining these entities are scarce and narrow in their scope. This paper reviews the evolution, development, and structure of the tooth and provides a summary of genodermatoses with aberrant dental findings. The latter are classified according to the abnormal dental findings: periodontal disease, anodontia/oligodontia/hypodontia, polydontia, enamel hypoplasia, natal teeth, dental pits, and others. Finally, we provide an algorithm that dermatologists and dentists can follow to better recognize genodermatoses with dental involvement.

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Section: Molecular Pathways In Tooth Developmentmentioning

confidence: 99%

Genodermatoses with teeth abnormalities

et al. 2020

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Oral Mucosa and Nails in Genodermatoses: A Diagnostic Challenge

Cantile

Coppola

Caponio

et al. 2021

JCM

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Genodermatoses represent a group of uncommon, hereditary, single-gene skin disorders, characterized by multisystem involvement, heterogeneous clinical manifestations and different degrees of morbidity and mortality. Some genodermatoses may have oral mucosa and nail involvement, since the oral cavity and cutaneous organ system, including nails, share a close embryologic origin. Nail disorders can manifest with nail hypoplasia or nail hypertrophy. Clinical pictures of affected oral mucosa can be extremely heterogeneous, ranging from asymptomatic papules to painful blisters, leukokeratosis, oral papillomas and fibromas to oral potentially malignant disorders and cancerous lesions. Oral mucosa and nails pathological features may occur synchronously or not and are usually associated with other systemic and skin manifestations. In some cases, oral mucosa and nails diseases may be distinct and constitute the principal sign of the genetic disorder, in other cases they represent only a part of the puzzle for the confirmation of the diagnosis. Continued awareness of the correlation between oral mucosa and nails findings can help physicians to diagnose genodermatosis in a timely manner, allowing more effective clinical management and prevention and/or early detection of complications. This article provides an overview of all specific genodermatoses affecting both oral mucosa and nails. Moreover, the correlation between teeth and nails is summarized in tabular form.

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Long‐term dental management of a patient with features of Schöpf–Schulz–Passarge syndrome

Cited by 2 publications

References 26 publications

Genodermatoses with teeth abnormalities

Genodermatoses with teeth abnormalities

Oral Mucosa and Nails in Genodermatoses: A Diagnostic Challenge

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