Results 11 to 20 of about 19,066 (210)

Ectodermal dysplasia

open access: yesČeská Stomatologie a Praktické Zubní Lékařství, 2013
Background: Ectodermal dysplasia is a rare, genetically determined disease, which is characterized by alterations in two or more ectodermal structures, at least one of these involving alterations in hair, teeth, nails, or sweat glands.
L. Kramerová, E. Kaplová
doaj   +1 more source

Apeced in Turkey: a case report and insights on genetic and phenotypic variability [PDF]

open access: yes, 2018
APECED is a rare monogenic recessive disorder caused by mutations in the AIRE gene. In this manuscript, we report a male Turkish patient with APECED syndrome who presented with chronic mucocutaneous candidiasis associated with other autoimmune ...
Alessandra Fierabraccia   +4 more
core   +1 more source

A Retrospective Study of Clinical and Mutational Findings in 45 Danish Families with Ectodermal Dysplasia [PDF]

open access: yes, 2014
Ectodermal dysplasias form a complex, nosologic group of diseases with defects in at least 2 ectodermal structures. A retrospective study of patients with ectodermal dysplasia seen at our department over a period of 19 years (1994-2013) was performed ...
Bygum, Anette   +4 more
core   +1 more source

Remember the periroot sheet in orthodontic treatment of ectodermal dysplasia patients

open access: yesDental Hypotheses, 2014
Introduction: Root resorption has various etiologies. Recent studies have demonstrated a periroot sheet covering the root. The outermost layer of this sheet is the Malassez′ epithelial layer. Tooth malformations are seen in ectodermal dysplasia and it is
Izabella Vest Hansen   +2 more
doaj   +1 more source

Prosthodontic management of hypohidrotic ectodermal dysplasia: a case report [PDF]

open access: yes, 2015
Introduction: Ectodermal dysplasia (ED) is a hereditary disorder associated with developmental disorders of two or more structures of ectodermal embryonic origin.
Bajraktarova, B.   +6 more
core   +3 more sources

Christ Siemens Touraine syndrome: Two case reports and felicitous approaches to prosthetic management

open access: yesContemporary Clinical Dentistry, 2015
Ectodermal dysplasia is a heterogeneous group of inherited disorders, which exhibit a classic triad of hypohydrosis, hypotrichosis, and hypodontia. Hypohidrotic or anhidrotic ectodermal dysplasia or Christ Siemens Touraine syndrome is the most common ...
Navanith Renahan   +3 more
doaj   +1 more source

Removable prosthetic treatment of an ectodermal dysplasia patient: A case report

open access: yesJournal of Craniomaxillofacial Research, 2020
Ectodermal dysplasia is an inherited disorder with partial or complete anodontia. Early dental treatments are mandatory for improving child mastication, communication, and esthetic.
Faezeh Atri   +2 more
doaj   +1 more source

Dental Management of Hypohydrotic Ectodermal Dysplasia: A Case Report [PDF]

open access: yesJournal of Mashhad Dental School, 2020
Introduction: Ectodermal dysplasia is a genetic rare disease, consisting of a group of abnormalities which are the results of the abnormal development of two or more embryonic ectoderm derivatives, such as the skin, hair, nail, sweat gland, tooth, and ...
Koorosh teymoornezhad   +2 more
doaj   +1 more source

Hypohidrotic Ectodermal Dysplasia with total anodontia: a case report [PDF]

open access: yes, 2011
Ectodermal dysplasia is a hereditary disorder that occurs as a consequence of disturbances in the ectoderm of the developing embryo. The triad of nail dystrophy, alopecia or hypotrichosis and palmoplantar hyperkeratosis is usually accompanied by a lack ...
Sathyajith Naik, N.   +3 more
core   +1 more source

Hay-Wells syndrome: Report of a rare disorder with dental management

open access: yesJournal of Indian Academy of Oral Medicine and Radiology, 2015
Hay-Wells syndrome is a rare autosomal dominant disorder characterized by ankyloblepharon, ectodermal dysplasia, and cleft palate and/or cleft lip [ankyloblepharon-ectodermal dysplasia-clefting (AEC) syndrome].
Sonal B Dudhia   +2 more
doaj   +1 more source

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