Results 11 to 20 of about 8,171 (177)

Prenatal ultrasound findings of ectodermal dysplasia: a case report

open access: yesBMC Pregnancy and Childbirth, 2022
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
doaj   +1 more source

Presentation of hypohidrotic ectodermal dysplasia in two siblings

open access: yesJournal of Indian Academy of Oral Medicine and Radiology, 2015
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
doaj   +1 more source

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

Ectodermal dysplasia: a narrative review of the clinical and biological aspects relevant to oral health [PDF]

open access: yesFrontiers in Pediatrics
Morandini AC   +11 more
exaly   +2 more sources

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

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

Evaluation of Ectodermal Dysplasia

open access: yesThe Kaohsiung Journal of Medical Sciences, 2006
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

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

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

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