Results 11 to 20 of about 8,171 (177)
Prenatal ultrasound findings of ectodermal dysplasia: a case report
Background Ectodermal Dysplasia is a diverse group of inherited disorders characterized by a congenital defect in two or more ectodermal structures. Due to a fairly low incidence, to the best of our knowledge there are few clues that can assist in making
Liang Li +3 more
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Presentation of hypohidrotic ectodermal dysplasia in two siblings
Ectodermal dysplasias are a large hereditary group of disorders which are usually manifested as X-linked recessive disorders and have a full expression in males, whereas females show little to no signs of the disorder.
Uday Ginjupally +3 more
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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
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Ectodermal dysplasia: a narrative review of the clinical and biological aspects relevant to oral health [PDF]
Morandini AC +11 more
exaly +2 more sources
Remember the periroot sheet in orthodontic treatment of ectodermal dysplasia patients
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
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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
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Removable prosthetic treatment of an ectodermal dysplasia patient: A case report
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
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Evaluation of Ectodermal Dysplasia
This case series report outlines possible cranio‐maxillofacial deformation consequences associated with ectodermal dysplasia (ED) and embryonic malformations, including dental agenesis. Also described are the oral aspects and rehabilitation. A total of 14 ED patients (7 males and 7 females, aged 5‐45 years) underwent clinical examination before ...
Başkan, Zelal +7 more
openaire +3 more sources
Hay-Wells syndrome: Report of a rare disorder with dental management
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
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Dental Management of Hypohydrotic Ectodermal Dysplasia: A Case Report [PDF]
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
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