Results 61 to 70 of about 4,786 (283)
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
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
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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
Anodontia Detected by Prenatal Sonography: A Case Report
, 2020 Anodontia is a rare orofacial complex developmental malformation. In contrast to normal tooth germ with roundhypo echogenic structure arranged in an arch-like manner in alveolar bone, anodontia shows an arch-like hyper echogenic structure without any ...
J. Sun, H. Zhang, Z. Yang
semanticscholar +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
Kepadatan kerang lumpur Anodontia edentula Linnaeus, 1758 kaitannya dengan parameter lingkungan di Kabupaten Muna [PDF]
, 2016 The research aims to analyze the density of mud clams Anodintia edentula Linnaeus, 1758 relation to environmental parameters, covering organic material content and composition of sediment in Muna regency. Research carried out in coastal Lambiku and Tobea
Omar, Sharifuddin Bin Andy +2 more
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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
Recreating the missing smile: A case report on ectodermal dysplasia
SRM Journal of Research in Dental Sciences, 2012 Ectodermal dysplasia syndrome is a group of hereditary disorders affecting the structures developing from the ectoderm. More than 150 different types have been described with the most common being the hypohidrotic and the hidrotic types.
R Shakila +3 more
doaj +1 more source