Ectodermal Dysplasia- A Case Report [PDF]
Ectodermal dysplasia is a hereditary genetic disorder that manifests various in one or more ectodermal derivatives such as skin ,nails, hair ,teeth ,exocrine glands and sebaceous glands ,the incidence of ectodermal dysplasia is rare 1 in 100000 ...
N. Jacob Prasanth, Aron Arun Kumar Vasa, Suzan Sahana, D. Sree Pranathi, CH. Sravani, R. Sruthi
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Dental Management of Ectodermal dysplasia: A case report [PDF]
A variety of syndromes/disorders (genetic/acquired) are encountered in our day-to-day life. Among them, ectodermal dysplasia is a rare syndrome which is transmitted as x-linked recessive/dominant disorder and is known to majorly affect males as compared ...
Joshi, Bharat +3 more
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Restoration of Oral Function for Adult Edentulous Patients with Ectodermal Dysplasia: A Prospective Preliminary Clinical Study [PDF]
, 2015 BackgroundTherapy with zygomatic implants (ZIs) or conventional implants (CIs) has proven to be an effective method to restore oral function for systemically healthy patients.
Huang, Wei +7 more
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Ellis-van Creveld with an Unusual Dental Anomaly: A Case Report
Iranian Journal of Medical Sciences, 2017 The Ellis-van Creveld (EVC) syndrome is a chondroectodermal dysplasia and is characterized by the cardinal features of disproportionate short stature, polydactyly, hidrotic ectodermal dysplasia, and congenital heart malformations, along with other ...
Suzanne Tanya Nethan +2 more
doaj
Early prosthetic rehabilitation of a juvenile patient with hereditary ectodermal dysplasia – a case report [PDF]
, 2015 Ectodermal dysplasia is the term used to describe a large and heterogenic group of congenital disorders. Ectodermal dysplasia affects at least two ectoderm-derived structures.
Bruziewicz-Mikłaszewska, Barbara +2 more
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Molecular interaction of connexin 30.3 and connexin 31 suggests a dominant-negative mechanism associated with erythrokeratodermia variabilis [PDF]
, 2017 Connexins are homologous four-transmembrane-domain proteins and major components of gap junctions. We recently identified mutations in either GJB3 or GJB4 genes, encoding respectively connexin 31 (Cx31) or 30.3 (Cx30.3), as causally involved in ...
Hohl, Daniel +4 more
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Schöpf-Schulz-Passarge syndrome: further delineation of the phenotype and genetic considerations. [PDF]
, 2008 Schöpf-Schulz-Passarge syndrome is a rare ectodermal dysplasia, characterized chiefly by multiple eyelid apocrine hidrocystomas, palmo-plantar keratoderma, hypodontia, hypotrichosis and nail dystrophy.
Annessi G. +4 more
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Hypohidrotic Ectodermal Dysplasia: A Case Report. [PDF]
Cureus, 2023 Shamim H, Hanif S.
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Opciones de tratamiento prótésico en niños con oligodoncias por displasia ectodérmica hidrótica [PDF]
, 2014 La reposición de los dientes no solamente influye en la adecuada alimentación y fonética, sino que también mejora la sonrisa y la apariencia personal, además del aspecto positivo que produce en el estado de salud psicológico y emocional de los niños ...
Beatriz García Alpízar +3 more
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