Results 11 to 20 of about 18,314 (251)

Anhydrotic Ectodermal Dysplasia [PDF]

open access: bronzeProceedings of the Royal Society of Medicine, 1966
R S Wells
openaire   +4 more sources

Ectodermal dysplasia

open access: yesMedical Journal of Dr. D.Y. Patil Vidyapeeth, 2018
Panduranga Chikkannaiah
doaj   +2 more sources

Prosthodontic Rehabilitation of a Female Child with Ectodermal Dysplasia

open access: yesJournal 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
doaj   +1 more source

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

Ectrodactyly-ectodermal dysplasia clefting syndrome (EEC syndrome)

open access: yesJournal 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
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

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

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

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

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