, 2006 Published as part of Cosel, Rudo von, 2006, Taxonomy of tropical West African bivalves. VI. Remarks on Lucinidae (Mollusca, Bivalvia), with description of six new genera and eight new species, pp.
Cosel, Rudo von
openaire +3 more sources
Prevalence and Patterns of Permanent Tooth Agenesis in Patients With Crouzon or Apert Syndrome: A Systematic Review and Meta-Analysis. [PDF]
Orthod Craniofac ResABSTRACT Crouzon and Apert syndromes are rare syndromic craniosynostoses frequently associated with craniofacial and dental anomalies, including tooth agenesis. Although individual studies have reported tooth agenesis prevalence data in specific populations, no attempts have been made to systematically synthesise these data.
Becerril Santos MC +3 more
europepmc +2 more sources
De Novo Missense Variant in TP63 Gene: Insights on Clinical and Molecular Investigations. [PDF]
J Gene MedWe report a heterozygous missense variant (c.184G〉C, p.Val62Leu) in exon 2 of the TP63 gene in a male patient with ectodermal dysplasia characterized by hypohidrosis, sparse hair, tooth agenesis, cleft lip/palate, hearing loss, and syndactyly. The variant was absent from public databases and unaffected relatives.
Chen J, Xi X, Xu X, Lin Y.
europepmc +2 more sources
Full Mouth Rehabilitation of an Adolescent Patient with Ectodermal Dysplasia: A Case Report [PDF]
Journal of South Asian Association of Pediatric Dentistry, 2022 Ectodermal dysplasia comprises genetic disorders of divergent groups that include dystrophies of ectodermally derived structures and their accessory structures, including hair, glands, teeth, skin, and nails.
Amith Adyanthaya +5 more
doaj +1 more source
Ectodermal Dysplasia with Partial Anodontia: A Case Report and Review [PDF]
, 2019 Ectodermal dysplasia is an X-Linked, recessive hereditary disease characterized by dysplasia of tissues of ectodermal origin. In Hypohidrotic Ectodermal Dysplasia (HED) males are more affected than female .The incidence of ectodermal dysplasia is rare (1
Tarun Vyas, Satish Bhosale
core +1 more source
NUMERIC DENTAL ANOMALIES IN CHILDREN FROM CLUJ-NAPOCA [PDF]
Romanian Journal of Stomatology, 2018 Numeric tooth anomalies involving a fewer number of teeth (hypodontia) are considered dental dystrophies determined by disturbances during the odontogenesis stage.
Viorica Ţărmure +8 more
doaj +1 more source
Hereditary Hypohidrotic Ectodermal Dysplasia: Report of a Rare Case [PDF]
Journal of Clinical and Diagnostic Research, 2013 Hereditary Hypohidrotic Ectodermal Dysplasia (HHED), an X-linked, recessive, Mendelian character, is seen usually in males and it is inherited through female carriers.
Geetha Paramkusam +3 more
doaj +1 more source
Step Wise Management of Asyndromic Tooth Agenesis with Ankyloglossia: A Case Report [PDF]
Journal of Clinical and Diagnostic Research, 2021 Ankyloglossia or tongue tie refers to restricted tongue movements, diagnosed in early childhood and adolescence that may cause changes in bone growth and other orofacial tissues results in altered oral functions of the child.
Vandana R Gadve, Vijaya S Dhote
doaj +1 more source
Primary Teeth Supported Fixed Prosthesis—A Predictable Treatment Alternative
Children, 2022 Background: Individuals with tooth agenesis often present a significant clinical challenge for dental practitioners. This retrospective study evaluated clinical and radiological long-term functional and esthetic outcomes following restoration using ...
Sarit Naishlos +8 more
doaj +1 more source
DCAF17 Mutation in Woodhouse-Sakati Syndrome: A Case Report on a Novel Homozygous Variant. [PDF]
Case Rep PediatrBackground: 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.
Khalili Dehkordi A, Vakili R.
europepmc +2 more sources