Results 71 to 80 of about 4,755 (272)
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
Familial cases of missing mandibular incisor: three case presentations [PDF]
, 1999 Hypodontia is the congenital absence of one or more teeth because of agenesis. The most commonly missing teeth are the third molars, the maxillary lateral incisors and the second premolars.
Ngeow, Dr. W.C.
core
Correlation of dental and chronological maturity in girls and boys aged 7 to 14 years [PDF]
, 2005 The aim of the study was to assess correlation level of dental and chronological maturity related to gender in a group of children of our population. Material and method: Total number of 320 girls and boys, 7 to 14 years old, participated in the study ...
Marković Evgenija +2 more
core +1 more source
Prosthetic rehabilitation of a young patient with Hypophosphatasia - A review and case report
Contemporary Clinical Dentistry, 2012 Hypophosphatasia is a congenital disease characterized by deficiency of serum and tissue non-specific alkaline phosphatase activity. The disease occurs due to mutations in the liver/bone/kidney alkaline phosphatase gene.
Partapjot S Grewal, Kanu Priya Gupta
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
, 2020 About 30 – 60% of patients complain on malfunctioning removable laminar dentures whatever the manufacturing method was chosen. An alternative method to correct complete anodontia is the construction of fixed implant-retained prostheses.
B. Pelekhan, M. Rozhko, L. Pelekhan
semanticscholar +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
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
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
Chromosomal assignment of the ovine hairless (hr) gene by fluorescence in situ hybridization. [PDF]
, 2008 Congenital hypotrichosis in mammalian species consists of partial or complete absence of a hair coat at birth. Affected individuals having a partial hair coat at birth may loose it subsequently.The aim of this paper was to physically map the ovine hr
Budelli E +6 more
core +1 more source