Management of Amelogenesis Imperfecta in Childhood: Two Case Reports

Möhn, Mirja; Bulski, Julia Camilla; Krämer, Norbert; Rahman, Alexander; Schulz‐Weidner, Nelly

doi:10.3390/ijerph18137204

Cited by 13 publications

(10 citation statements)

References 16 publications

Supporting

Mentioning

Contrasting

Order By: Relevance

“…Dentigerous cysts associated with impacted teeth in AI patients are rarely reported in the literature. During the mixed dentition period, Möhn M. et al discussed various management dentitions for AI patients [ 11 ]. Matthew L. et al and Tripathy M. et al reported a case of multiple periapical cysts in an AI patient and its management.…”

Section: Discussionmentioning

confidence: 99%

Role of Dental Professionals in the Management of a Dentigerous Cyst in a Patient With Amelogenesis Imperfecta

Chinnakutti¹,

Mohan²,

Murugesan³

et al. 2022

Cureus

View full text Add to dashboard Cite

Amelogenesis imperfecta (AI) is a hereditary condition that affects the clinical features and structure of the enamel. The enamel formation diseases are inherited and might be X-linked, autosomal dominant, recessive, sex-related, or sporadic. Dental professionals should evaluate such patients completely, both clinically and radiographically, to detect any cysts associated with impacted or unerupted teeth. This report describes the case of a 10-year-old patient affected by amelogenesis imperfecta with a dentigerous cyst involving an impacted tooth and an unerupted tooth of the maxilla.

show abstract

Section: Discussionmentioning

confidence: 99%

Role of Dental Professionals in the Management of a Dentigerous Cyst in a Patient With Amelogenesis Imperfecta

Chinnakutti¹,

Mohan²,

Murugesan³

et al. 2022

Cureus

View full text Add to dashboard Cite

show abstract

“…Conservative or prosthetic and orthodontic treatment via the use of crowns should be strongly necessary for oral rehabilitation. [145]…”

Section: Heimler Syndromementioning

confidence: 99%

Ocular Manifestations in Patients with Sensorineural Hearing Loss

Parameswarappa

Zaheer

Chhablani

et al. 2022

JOVR

View full text Add to dashboard Cite

(SNHL) can have a large impact on the outcome and treatment of pediatric patients. Due to the common co-incidence of ocular manifestations and SNHL in children, both ophthalmologic and hearing loss screening and routine examinations must be conducted to minimize adverse outcomes and worsening of pathology. Early evaluation and diagnosis is imperative for intervention and further development of the patient. Coincidence requires a thorough evaluation that includes a comprehensive history, examination, and diagnostic testing. In this article, a literature review was conducted to analyze the presentations of various diseases and syndromes, such as Alport Syndrome, Waardenburg Syndrome, Norrie Disease, Usher Disease, Stickler Syndrome, Marfan Syndrome, Congenital Rubella, and Hereditary Optic Neuropathies. We divided the various ocular pathologies into anterior and posterior segment presentations and associated systemic findings for better understanding. Additionally, this review aims to include an update on the management of patients with both ocular and hearing loss manifestations.

show abstract

“…A decrease in the occlusal vertical dimension (VDO) is often observed due to quick wear and deterioration of the dental structure. 11 However, each case is unique. Only a few case reports of AI rehabilitation have been reported, and even fewer report significant follow-up.…”

Section: Introductionmentioning

confidence: 99%

“…In particular, conservative, prosthetic and orthodontic treatment should be conducted together. A decrease in the occlusal vertical dimension (VDO) is often observed due to quick wear and deterioration of the dental structure 11 …”

Section: Introductionmentioning

confidence: 99%