Results 41 to 50 of about 3,300 (225)
American Journal of Medical Genetics Part A, Volume 200, Issue 4, Page 790-799, April 2026.ABSTRACT TSPEAR (chr. 21q22.3) encodes a protein involved in tooth development and is predominantly expressed in the enamel knot. Biallelic loss of function variants in TSPEAR cause ectodermal dysplasia, tooth agenesis and sensorineural hearing loss. However, the role of TSPEAR in auditory processes is unclear.
Debora Vergani +17 more
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
The Journal of Indian Prosthodontic Society, 2022 Treatment of pediatric patients with partial anodontia is a challenge requiring interdisciplinary approach. Growth period, reduced vertical dimension, microdontia, and unacceptable esthetics present difficulties at various stages of prosthetic ...
Natarajan Kalavathy +4 more
doaj +1 more source
International Journal of Dentistry, Volume 2026, Issue 1, 2026.Objective This study investigated the prevalence of dental anomalies within the athlete population in Qatar using panoramic radiographs. Design This retrospective, cross‐sectional study was conducted at Aspetar Hospital in Qatar. Materials and Methods Digital panoramic radiographs of 5000 records of athletes attending dental department were ...
Atef Hashem +6 more
wiley +1 more source
“Maxillary lateral incisor partial anodontia sequence”: a clinical entity with epigenetic origin
Dental Press Journal of OrthodonticsThe relationship between maxillary lateral incisor anodontia and the palatal displacement of unerupted maxillary canines cannot be considered as a multiple tooth abnormality with defined genetic etiology in order to be regarded as a “syndrome”.
Alberto Consolaro +2 more
doaj +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
Treatment with removable prosthesis in hypohidrotic ectodermal dysplasia : a clinical case [PDF]
, 2008 Ectodermal dysplasias form part of a wide range of syndromes presenting abnormal development of two or more tissues derived from the ectoderm. Hypohidrotic ectodermal dysplasia is a congenital syndrome, characterized by hypotrichosis (hair is sparse ...
Blanco-Moreno Alvarez-Buylla, Fernando +4 more
core
Anodontia - A Report of 2 Cases
Journal of Indian Academy of Oral Medicine and Radiology, 2004 True anodontia or congenital absence of the teeth may be of 2 types-total and partial. Total anodontia may involve both the deciduous and the permanent dentition.
K Bhuvana, Mubeen
doaj
Dental agenesis in cleft lip and/or palate pf the “Centro Pró-Sorriso” – Universidade José do Rosário Vellano [PDF]
RGO: Revista Gaúcha de Odontologia, 2008 Objective: Analyze periapical and panoramic radiographs in order to define the incidence of dental agenesis in carriers of cleft lip and/or cleft palate among patients of UNIFENAS “Centro Pró-Sorriso” (Pro-Smile Center) in Alfenas – MG.
Orivaldo Tavano +1 more
doaj
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