Results 41 to 50 of about 1,605 (178)
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
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
Contemporary Clinical Dentistry, 2016 Missing teeth are a common developmental abnormality in humans. It may manifest as absence of varying numbers of primary and/or secondary teeth. Early treatment and follow-up are the key to successful rehabilitation of young patients with congenitally ...
Manu Rathee +3 more
doaj +1 more source
, 2004 Anodontia ovum (Reeve, 1850) Habitat (inferred). Burrows in sand and muddy sand often associated with sea-grass beds from low in the littoral and sublittoral. Distribution. Shells and valves were frequently recorded throughout the lagoon but not in large numbers. Remarks.
Oliver, P. Graham +4 more
openaire +2 more sources
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
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
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
Dental Abnormalities in Congenital Ichthyoses: Case Report and Review of the Literature
Pediatric Dermatology, Volume 42, Issue 2, Page 305-310, March/April 2025.ABSTRACT We describe a 1‐day old female with features of keratitis‐ichthyosis‐deafness (KID) syndrome and natal teeth. Genetic analysis confirmed GJB2 263C and A88V de novo pathogenic variants consistent with KID syndrome. Natal teeth were promptly extracted to avoid the risk of aspiration.
Sarah Maarouf +3 more
wiley +1 more source
Outcome of Single Dental Implants Over 38–40 Years: A Long‐Term Follow‐Up Study
Clinical Implant Dentistry and Related Research, Volume 27, Issue 1, February 2025.ABSTRACT Introduction This is a comprehensive, long‐term follow‐up study of single‐implant treatments. At the Brånemark Clinic in Gothenburg, Sweden, during the period of 1982–1985, 16 patients received single‐tooth implants. Objective This study evaluates the survival rate of the implants after nearly four decades, focusing on the biological and ...
Sargon Barkarmo, Jan Kowar
wiley +1 more source
Hypohidrotic Ectodermal Dysplasia [PDF]
Journal of Clinical and Diagnostic Research, 2021 Chiranjit Ghosh +2 more
doaj +1 more source