Results 61 to 70 of about 2,260 (205)
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
Hypodontia in the permanent dentition: a study of its prevalence in Malaysian children
Australasian Orthodontic Journal, 1989 An investigation of the prevalence and distribution of hypodontia was carried out in Malaysian children between the ages of five to fifteen years. Hypodontia occurred in 2.8 per cent of these children.
Nik-Hussein Nik Moriah
doaj +1 more source
Displasia Ektodermal Hipohidrotik
Sari Pediatri, 2016 Seorang bayi laki-laki berusia 4 bulan menderita displasia ektodermal hipohidrotik (DEH), merupakan kelainan genetik yang sebagian besar diturunkan secara x-linked recessive.
Eveline PN +2 more
doaj +1 more source
Oligodontia Management in a Resource‐Limited Setting: Two Case Reports and Review of Literature
Case Reports in Dentistry, Volume 2025, Issue 1, 2025.Introduction: Oligodontia represents the developmental absence of six or more teeth, posing significant challenges for masticatory function, speech, and psychosocial well‐being. While extensively documented in developed countries, limited reports exist from resource‐constrained settings in Africa.
A. B. Malami +7 more
wiley +1 more source
Frequency, prevalence and treatment methods of anodontia and supernumbered teeth [PDF]
, 2023 Universitatea de Stat de Medicină şi Farmacie „Nicolae Testemiţanu”, Chişinău, Republica MoldovaIntroducere. Anodonțiile și dinții supranumerari sunt anomalii dentare de număr, care se întâlnesc cu o frecvență de la 0,5% până la 12,5%.
Stepco, Elena, Globa, Mihai
core +1 more source
Case Reports in Dentistry, Volume 2025, Issue 1, 2025.Introduction Ellis–van Creveld (EVC) syndrome, also known as chondroectodermal dysplasia, is a rare autosomal recessive disorder that affects multiple embryonic tissues. It is primarily caused by mutations in the EVC gene. Patient Information We report an 11‐year‐old male diagnosed with EVC syndrome, who carries a novel homozygous pathogenic mutation ...
Mahnegar Shariati +4 more
wiley +1 more source
, 2011 Ectodermal dysplasias are a complex group of genetically determined disorders clinically characterized by congenital alterations of the structures derived from the ectoderm.
Sholapurkar, Amar A. +2 more
core +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
DCAF17 Mutation in Woodhouse–Sakati Syndrome: A Case Report on a Novel Homozygous Variant
Case Reports in Pediatrics, Volume 2025, Issue 1, 2025.Background: Woodhouse–Sakati syndrome (WSS) is a rare autosomal recessive disorder characterized by a constellation of symptoms, including alopecia, hypogonadism, diabetes, mental retardation, and extrapyramidal syndrome. Here, we present a case study of a girl with WSS, focusing on clinical features, genetic analysis, and treatment.
Asal Khalili Dehkordi +2 more
wiley +1 more source
Anodontia (Loripinus) senegalensis Cosel 2005
, 2006 Anodontia (Loripinus) senegalensis Cosel in Taylor & Glover, 2005 (Figs 21C, D; 22) Anodontia (Loripinus) senegalensis Cosel in Taylor & Glover, 2005: 326, figs 11B, 12B, 42F-I, 43. TYPE MATERIAL.
Cosel, Rudo von
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