Results 11 to 20 of about 19,360 (251)
Prosthodontic Rehabilitation of a Female Child with Ectodermal Dysplasia
Journal of the Dow University of Health Sciences, 2021 Ectodermal Dysplasia (ED) is an X-linked inherited disorder with male predominance. Female patients may show partial expression of Ectodermal Dysplasia. Significant findings include hypodontia, hyposalivation, protuberant lips, conical teeth and loss of
Aleshba Saba Khan +2 more
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Prenatal ultrasound findings of ectodermal dysplasia: a case report
BMC 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
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Ectrodactyly-ectodermal dysplasia clefting syndrome (EEC syndrome)
Journal of Oral Biology and Craniofacial Research, 2014 Ectrodactyly-ectodermal dysplasia- clefting syndrome (also k/a. split hand- split foot malformation /split hand-split foot ectodermal dysplasia- cleft syndrome/ectodermal dysplasia cleft lip/cleft palate syndrome) a rare form of ectodermal dysplasia, is ...
Monika Koul +2 more
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Presentation of hypohidrotic ectodermal dysplasia in two siblings
Journal 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
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A Retrospective Study of Clinical and Mutational Findings in 45 Danish Families with Ectodermal Dysplasia [PDF]
, 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
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Apeced in Turkey: a case report and insights on genetic and phenotypic variability [PDF]
, 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
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Remember the periroot sheet in orthodontic treatment of ectodermal dysplasia patients
Dental 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
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Prosthodontic management of hypohidrotic ectodermal dysplasia: a case report [PDF]
, 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
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Contemporary 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
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Removable prosthetic treatment of an ectodermal dysplasia patient: A case report
Journal 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