• 'Double trouble': diagnostic challenges in genetic skin disorders
• A case report of hypohidrotic ectodermal dysplasia: A mini-review with latest updates
• A Family with EEC Syndrome in the Son and ADULT Syndrome in His Father Caused by the c.797G&gt;A (p.Arg266Gln) Pathogenic Variant in the <em>TP63</em> Gene
• A Mongolian patient with hypohidrotic ectodermal dysplasia with a novel P121S variant in EDARADD
• A novel chondroectodermal dysplasia mapped to chromosome 2q24.1-q31.1
• A Rare Case of Hypohidrotic Ectodermal Dysplasia in a Seven-Year-Old Child
• A simple prosthetic restorative solution of a single peg-shaped upper central primary incisor in a case of ectodermal dysplasia
• Absent meibomian glands and cone dystrophy in ADULT syndrome: identification by whole exome sequencing of pathogenic variants in two causal genes <em>TP63</em> and <em>CNGB3</em>
• Acro-Dermato-Ungual-Lacrimal-Tooth Syndrome: An Uncommon Member of the Ectodermal Dysplasias
• ADULT syndrome caused by a mutation previously associated with EEC syndrome
• ADULT syndrome due to an R243W mutation in TP63
• ADULT syndrome: dental features of a very rare condition
• ADULT syndrome: phenotype in a Brazilian family with the R298Q mutation
• Associations between ectodermal dysplasia, psychological distress and quality of life in a group of adults with oligodontia
• Autosomal dominant mutation of MSX1 gene causing tooth and nail syndrome
• Case report expanding the germline AXIN2- related phenotype to include olfactory neuroblastoma and gastric adenoma
• Case report: Early prosthetic treatment in children with ectodermal dysplasia
• Cerebral hemorrhage caused by shaking adult syndrome? Evidence from biomechanical analysis using 3D motion capture and finite element models
• Christ Siemens Touraine syndrome: A rare case report
• Christ-Siemens-Touraine Syndrome: A Report of a Rare Pediatric Case
• Cleft palate and ADULT phenotype in a patient with a novel TP63 mutation suggests lumping of EEC/LM/ADULT syndromes into a unique entity: ELA syndrome
• Clinical and Molecular Genetic Analysis of Cases with Ectodermal Dysplasia
• Clinical and molecular study in a child with X-linked hypohidrotic ectodermal dysplasia
• Confirmation of a Phenotypic Entity for <em>TSPEAR</em> Variants in Egyptian Ectodermal Dysplasia Patients and Role of Ethnicity
• Confirmation of a Phenotypic Entity for TSPEAR Variants in Egyptian Ectodermal Dysplasia Patients and Role of Ethnicity
• Conventional Complete Denture in Patients with Ectodermal Dysplasia
• Deleterious Variants in <em>WNT10A</em>, <em>EDAR,</em> and <em>EDA</em> Causing Isolated and Syndromic Tooth Agenesis: A Structural Perspective from Molecular Dynamics Simulations
• Dental and maxillofacial characteristics of six Japanese individuals with ectrodactyly-ectodermal dysplasia-clefting syndrome
• Dental management of ectodermal dysplasia: two clinical case reports
• Dental management of Rapp-Hodgkin syndrome associated with oral cleft and hypodontia
• Dentomaxillofacial characteristics of ectodermal dysplasia
• Ear nose throat manifestations in hypoidrotic ectodermal dysplasia
• Ectodermal dysplasia - A challenge for dentists
• Ectodermal dysplasia - Maxillary and mandibular alveolar reconstruction with dental rehabilitation: A case report and review of the literature
• Ectodermal dysplasia in identical twins
• Ectodermal Dysplasia Presenting as Heat Exhaustion in an Adolescent Boy
• Ectodermal dysplasia: a genetic review
• Ectodermal Dysplasia: Association with Anti-Basement Membrane Autoantibodies
• Ectodermal dysplasia: important role of complex dental care in its interdisciplinary management
• Ectodermal dysplasia: Report of two cases in a family and literature review
• Ectodermal dysplasias: Classification and organization by phenotype, genotype and molecular pathway
• Ectodermal dysplasias: the p63 tail
• EEC- and ADULT-associated TP63 mutations exhibit functional heterogeneity toward P63 responsive sequences
• EEC-LM-ADULT syndrome caused by R319H mutation in TP63 with ectrodactyly, syndactyly, and teeth anomaly: A case report
• Ektodermale Dysplasie
• Ellis van Creveld syndome
• Ellis van creveld syndrome: Cardiac anomalies and anesthetic implications
• Ellis-van Creveld Syndrome (chondro-ectodermal dysplasia) in two siblings
• Ellis-van Creveld syndrome: report of two cases
• Fixed prosthodontic rehabilitation for an adolescent patient with ectodermal dysplasia using a fully digital workflow: Two-year follow-up
• Functional characterization of a novel TP63 mutation in a family with overlapping features of Rapp-Hodgkin/AEC/ADULT syndromes
• Gene Mutations of the Three Ectodysplasin Pathway Key Players (<em>EDA</em>, <em>EDAR</em>, and <em>EDARADD</em>) Account for More than 60% of Egyptian Ectodermal Dysplasia: A Report of Seven Novel Mutations
• Gene Mutations of the Three Ectodysplasin Pathway Key Players (EDA, EDAR, and EDARADD) Account for More than 60% of Egyptian Ectodermal Dysplasia: A Report of Seven Novel Mutations
• Hypohidrotic ectodermal dysplasia - diagnostic aids and a report of 5 cases
• Hypohidrotic Ectodermal Dysplasia (ED): A Case Series
• Hypohidrotic ectodermal dysplasia associated with glucose-6-phosphate dehydrogenase deficiency
• Hypohidrotic ectodermal dysplasia with ankylosis of temporomandibular joint and cleft palate: A rare presentation
• Hypohidrotic Ectodermal Dysplasia: A Rare Disorder With Bilateral Infantile Glaucoma
• Hypohidrotic ectodermal dysplasia: A rare entity
• Hypohidrotic ectodermal dysplasia: clinical and molecular review
• Hypohydrotic Ectodermal Dysplasia in an Indian Family
• Implant-prosthetic partial-arch restoration in a patient with ectodermal dysplasia characterized by oligodontia and localized bone deficiency: a case report
• Implant-supported Oral Rehabilitation in Child with Ectodermal Dysplasia - 4-year Follow-up
• Improving the Quality of Life in Patients With Hypohidrotic Ectodermal Dysplasia: A Holistic Approach
• Infantile bilateral glaucoma in a child with ectodermal dysplasia
• JAAD Grand Rounds quiz. Palmoplantar keratoderma, hypodontia, hypotrichosis, nail dystrophy, and multiple eyelid cysts
• Management of a case of ectodermal dysplasia: a multidisciplinary approach
• MSX1 mutations and associated disease phenotypes: genotype-phenotype relations
• Mutations in AEC syndrome skin reveal a role for p63 in basement membrane adhesion, skin barrier integrity and hair follicle biology
• Mutations in the EDA gene are responsible for X-linked hypohidrotic ectodermal dysplasia and hypodontia in Chinese kindreds
• New observation of severe tooth malformation in a female patient with ectodermal dysplasia due to the EDA splice acceptor variant c.742-2A&gt;G
• New observation of severe tooth malformation in a female patient with ectodermal dysplasia due to the EDA splice acceptor variant c.742-2A>G
• Novel homozygous frameshift insertion variant in the last exon of the EDARADD causing hypohidrotic ectodermal dysplasia in two siblings: case report and review of the literature
• Oculodentodigital dysplasia
• Oligodontia ectodermal dysplasia--on signs, symptoms, genetics, and outcomes of dental treatment
• Oral and craniofacial manifestations of Ellis-van Creveld syndrome: Case series
• Oral Rehabilitation of a Child with Hypohidrotic Ectodermal Dysplasia
• Oral rehabilitation of a patient with ectodermal dysplasia with prosthodontics treatment
• Phenotypic Variation in Patients with Homozygous c.1678G&gt;T Mutation in EVC Gene: Report of Two Mexican Families with Ellis-van Creveld Syndrome
• Prosthetic rehabilitation of a child with Rapp-Hodgkin syndrome
• Prosthetic rehabilitation of a child with X-linked hypohidrotic ectodermal dysplasia: a case report and 12-month follow-up
• Prosthetic rehabilitation of a patient with ectrodactyly-ectodermal dysplasia-cleft lip/palate syndrome through a hybrid workflow: A case report with 2-year follow-up
• Prosthetic rehabilitation of an adolescent with hypohidrotic ectodermal dysplasia with partial anodontia: case report
• Prosthetic rehabilitation with fixed prosthesis of a 5-year-old child with Hypohidrotic Ectodermal Dysplasia and Oligodontia: a case report
• Prosthodontic management of a child with ectodermal dysplasia: a case report
• Prosthodontic Management of a Pediatric Patient with Christ-Siemens-Touraine Syndrome: A Case Report
• Prosthodontic rehabilitation of hereditary ectodermal dysplasia in an 11-year-old patient with flexible denture: a case report
• Rapp-Hodgkin syndrome: clinical and dental findings
• Schöpf-Schulz-Passarge syndrome with pili torti: A new association?
• Schöpf-Schulz-Passarge syndrome: further delineation of the phenotype and genetic considerations
• Shaken adult syndrome due to ocean wave: an autopsy case
• The effect of ectodermal dysplasia on volume and surface area of maxillary sinus
• Tricho-odonto-onycho-dermal dysplasia and WNT10A mutations
• Two novel heterozygous mutations of EVC2 cause a mild phenotype of Ellis-van Creveld syndrome in a Chinese family
• Unusual manifestations of ectodermal dysplasia-syndactyly syndrome type I in two Yemeni siblings
• Unusual presentation of a severe autosomal recessive anhydrotic ectodermal dysplasia with a novel mutation in the EDAR gene
• Witkop syndrome: A case report of an affected family
• Witkop tooth and nail syndrome: a report of three cases in a family
• Witkop's syndrome: A case report
• Witkop's tooth and nail syndrome: a multifaceted approach to dental management