Kongenitale bullöse Poikilodermie (Kindler‐Syndrom) – neue Mutation

Lennartz, L.; Has, Cristina; Lehmann, Percy

doi:10.1111/j.1610-0387.2012.08050_suppl.x

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Intraoral Soft Tissue Involvement1

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2020

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“…While some patients, particularly younger cases, do not report involvement of the oral mucosa, [173][174][175][176] others report few ulcers 164,177,178 and a third group presents fragile mucosa and painful ulcers scattered throughout the oral mucosa, affecting the alveolar ridge, soft palate, lip, and floor of the mouth. 133,162,164,165,179,180…”

Section: Intraoral Soft Tissue Involvementmentioning

confidence: 99%

Clinical practice guidelines: Oral health care for children and adults living with epidermolysis bullosa

Krämer

Lucas

Gamboa

et al. 2020

Special Care in Dentistry

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Background: Inherited epidermolysis bullosa (EB) is a genetic disorder characterized by skin fragility and unique oral features. Aims: To provide (a) a complete review of the oral manifestations in those living with each type of inherited EB, (b) the current best practices for managing oral health care of people living with EB, (c) the current best practices on dental implant-based oral rehabilitation for patients with recessive dystrophic EB (RDEB), and (d) the current best practice for managing local anesthesia, This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.

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