Results 71 to 80 of about 3,257 (209)

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, Sri Rezeki Hadinegoro, Siti Aisah Boediardja   +2 more
doaj   +1 more source

Oral Examination [PDF]

, 2017
The oral cavity is the first component of the digestive tract, which is delimited by the lips anteriorly and the oropharynx posteriorly. The oral cavity functions as a protective barrier and is an essential component for speech and swallowing ...
Burgess, Jeff, Eisen, Drore, Lynch, Denis P, Nordlund, James J., Stafford, Gary L, Villa, Alessandro, Wells, Michael J.   +6 more
core   +1 more source

Hereditary Colorectal Cancer and Polyposis Syndromes Caused by Variants in Uncommon Genes

Genes, Chromosomes and Cancer, Volume 63, Issue 8, August 2024.
ABSTRACT A substantial number of hereditary colorectal cancer (CRC) and colonic polyposis cannot be explained by alteration in confirmed predisposition genes, such as mismatch repair (MMR) genes, APC and MUTYH. Recently, a certain number of potential predisposition genes have been suggested, involving each a small number of cases reported so far. Here,
Ahmed Bouras, Aurélie Fabre, Hélène Zattara, Sandrine Handallou, Françoise Desseigne, Caroline Kientz, Fabienne Prieur, Magalie Peysselon, Clémentine Legrand, Laura Calavas, Jean‐Christophe Saurin, Qing Wang   +11 more
wiley   +1 more source

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, Leandro Carnevalli Franco de Carvalho   +1 more
doaj  

CATSHL syndrome, a new family and phenotypic expansion

Clinical Genetics, Volume 105, Issue 3, Page 313-316, March 2024.
A novel heterozygous variant of FGFR3 was identified in 2 members of the same family affected by CAmptodactyly – Tall stature – Scoliosis – Hearing Loss (CATSHL) syndrome with some shared features with Lacrimo – Auricolo – Dento – Digital (LADD) syndrome. LADD and CATSHL syndromes could be further evidences of high pleiotropy of FGFR3.
Silvia Cannova, Camilla Meossi, Federico Grilli, Donatella Milani, Federica Alberti, Claudia Cesaretti, Paola Giovanna Marchisio, Francesca Crosti, Lidia Pezzani   +8 more
wiley   +1 more source

Characterization of novel MSX1 variants causally associated with non‐syndromic oligodontia in Chinese families

Molecular Genetics &Genomic Medicine, Volume 12, Issue 1, January 2024.
We ascertained three new MSX1 variants in three unrelated Chinese non‐syndromic oligodontia (NSO) families: one insertion variant (c.576_577insTAG (p. Gln193 *)) and two missense variants (c.871T>C (p.Tyr291His); c.644A>C (p.Gln215Pro)). Immunofluorescence analysis revealed that truncated MSX1 (p. Gln193*) localized in the cytoplasm.
Ya Zhao, Jiabao Ren, Lingqiang Meng, Yan Hou, Chunyan Liu, Guozhong Zhang, Wenjing Shen   +6 more
wiley   +1 more source

Anhidrotic Ectodermal Dysplasia in a Child Due to a Rare Mutation in the EDA Gene (a Clinical Case)

Журнал медико-биологических исследований
Anhidrotic 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, Tatyana Yu. Gagarina, Nadezhda G. Davydova   +2 more
doaj   +1 more source

Customized Prosthetic Oral Rehabilitation of a Child with Hypohidrotic Ectodermal Dysplasia: A Case Report [PDF]

Journal of South Asian Association of Pediatric Dentistry
The present case report describes interdisciplinary prosthetic oral rehabilitation of a 7-year-old male child presenting classical features of hypohidrotic ectodermal dysplasia (HED) and subtotal anodontia. The treatment, in this case, was simplified and
Hitesh Chander Mittal, Sudhir Bhandari, Ashima Goyal, Aditi Kapur, Krishan Gauba   +4 more
doaj   +1 more source

Abordagem clínica de pacientes com síndrome de Down em medicina dentária [PDF]

, 2015
Projeto de Pós-Graduação/Dissertação apresentado à Universidade Fernando Pessoa como parte dos requisitos para obtenção do grau de Mestre em Medicina DentáriaO presente trabalho tem como objetivo a análise sobre a abordagem clinica de pacientes com ...
Silva, José Diogo Rodrigues da
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