Results 21 to 30 of about 4,755 (272)
Oral Rehabilitation in a Child with Anodontia Case Report [PDF]
Biomedical Journal of Scientific & Technical Research, 2018 Anodontia is an inherited genetic disorder and is associated withectodermal dysplasia. Oral rehabilitation procedures are helping clinicians restore patients to better function and more esthetic outcomes than ever before.
Irina Totolici +2 more
openaire +2 more sources
Primary double tooth with partial anodontia of permanent dentition - a case report [PDF]
, 2010 Dental anomalies of number and forms may occur in the primary and permanent dentition. Various terms have been used to describe dental twinning anomalies: gemination, fusion, concrescence, double teeth, cojoined teeth, twinned teeth ...
VA. Prasad Rao +5 more
openalex +2 more sources
Ectodermal dysplasia and partial anodontia: A case report
Journal of Medical and Scientific Research, 2015 Ectodermal dysplasia is a hereditary disorder that occurs as a consequence of disturbances in the ectoderm of the developing embryo. It is usually accompanied by lack of sweat glands and a partial or complete absence of primary and/or permanent dentition.
Prasad M
doaj +3 more sources
A Case of Partial Anodontia [PDF]
Journal of the Royal Army Medical Corps, 1967 G.D. Stafford
openalex +4 more sources
Revista portuguesa de estomatologia e cirurgia maxilo-facial, 2020 J. Perdigão, J. Ramos
openalex +2 more sources
Partial Anodontia-An Untold Clinical Presentation of Diamond Blackfan Anaemia: Case Report
Journal of Clinical and Diagnostic Research, 2019 K. Shanthi +3 more
openalex +2 more sources
A case of anodontia with ectodermal dysplasia on the siblings
Japanese Journal of Oral & Maxillofacial Surgery, 1980 Kazuya Motomura +4 more
openalex +3 more sources
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