Results 51 to 60 of about 3,300 (225)
Pigmentary Mosaicism: An Overview
JEADV Clinical Practice, Volume 4, Issue 3, Page 681-689, August 2025.Pigmentary mosaicism is reflected by a patterned hypo‐, hyperpigmentation, or both combined in cutis tricolour. Pigmentary mosaicism can be associated with extracutaneous features (mainly neurological, musculoskeletal or ophthalmological). Three main mechanisms are involved in the development of pigmentary mosaicism: mosaicism for a chromosomal ...
C. Colmant +3 more
wiley +1 more source
Revista da Faculdade de Odontologia de Porto Alegre, 2009 The objective of the present article is to report an uncommon case of a boy with history of 11 natal lost teeth, all belonging to the normal series of primary dentition, associated with absence of up to 21 permanent tooth germs. Such a condition resulted
Patricia Fernanda Dias +3 more
doaj +1 more source
Paediatric Hypotrichosis: A Clinical and Algorithmic Approach to Diagnosis
Australasian Journal of Dermatology, Volume 66, Issue 3, Page e109-e119, May 2025.ABSTRACT Paediatric hypotrichosis is the clinical feature of paucity of hair arising congenitally or in early life with the presentation being that of the child whose hair is growing insufficiently. It is a hallmark finding of a diverse group of genodermatoses and sporadic disorders, presenting as either an isolated symptom or in association with ...
Neda So, Leona Yip, David Orchard
wiley +1 more source
Anhidrotic Ectodermal Dysplasia in a Child Due to a Rare Mutation in the EDA Gene (a Clinical Case)
Журнал медико-биологических исследованийAnhidrotic ectodermal dysplasia is а heterogenous genetic disorder with multiple clinical manifestations. In medical examinations, including dental examinations, the differential aspect of diagnosis is important, since many forms of the disease have ...
Sergey N. Levitskiy +2 more
doaj +1 more source
The Incidence of Tooth Agenesis in Pediatric Patients in the Olomouc Region
Česká Stomatologie a Praktické Zubní Lékařství, 2014 Aim of the study: Many developmental anomalies can occur in craniofacial region. Dental developmental anomalies, namely hypodontia, are the most often of them.
L. Kramerová +3 more
doaj +1 more source
Retardo en la erupción dental en adolescentes con hipotiroidismo [PDF]
, 2012 OBJECTIVE: To report the case of an adolescent with undiagnosed hypothyroidism who sought dental clinic care due to delayed tooth eruption. Multiprofessionalwork enabled the diagnosis.
Braga, Josefina Aparecida Pellegrini +3 more
core +4 more sources
Clinical Oral Implants Research, Volume 36, Issue 4, Page 505-517, April 2025.ABSTRACT Objectives WNT10A mutations are associated with tooth agenesis. This study aimed to assess the clinical outcomes of dental implants in patients carrying WNT10A mutations with different molecular statuses and phenotypes over a long‐term follow‐up period. Materials and Methods Patients with tooth agenesis were screened by whole‐exome sequencing (
Jiaqi Dou +6 more
wiley +1 more source
A Study on Partial Anodontia with and without Syndromes
Journal of Indian Academy of Oral Medicine and Radiology, 2004 Man has 32 teeth in his permanent set. Many persons fail to develop one or more of their third molars, thereby causing the numbers of teeth to lie between 28 and 32. A small percentage of persons also fail to develop even that allotted number.
Bhavin Dudhia, Jigna Shah
doaj
Prosthetic dental management of a patient with anhidrotic ectodermal dysplasia. A Case Report.
Journal of Oral Research, 2021 Introduction: Ectodermal dysplasia (ED) comprises a broad group of genetic disorders characterized by alterations of the structures derived from the ectoderm, including those of the stomatognathic system.
Daniel Hernández-González +1 more
doaj +1 more source
Erupted Complex Odontoma Mimicking a Mandibular Second Molar [PDF]
, 2015 Complex odontoma (CO) is considered one of the most common odontogenic lesions, composed by a miscellaneous of dental tissue such as enamel, dentin, pulp and sometimes cementum.
Almeida, Luis Eduardo +4 more
core +1 more source