scholarly journals A novel EDA variant causing X-linked hypohidrotic ectodermal dysplasia: Case report

2021 ◽  
Vol 29 ◽  
pp. 100796
Author(s):  
Baiba Alksere ◽  
Liene Kornejeva ◽  
Ieva Grinfelde ◽  
Aigars Dzalbs ◽  
Dace Enkure ◽  
...  
2015 ◽  
Vol 14 (3) ◽  
pp. 10344-10351 ◽  
Author(s):  
S.X. Huang ◽  
J.L. Liang ◽  
W.G. Sui ◽  
H. Lin ◽  
W. Xue ◽  
...  

2003 ◽  
Vol 27 (1) ◽  
pp. 5-8 ◽  
Author(s):  
Ekaterini Paschos ◽  
Karin Christine Huth ◽  
Reinhard Hickel

Ectodermal dysplasia is a rare hereditary disorder with a characteristic physiognomy. The case of a 5-year-old child with hypohidrotic ectodermal dysplasia and complete anodontia is presented. Because of the anodontia and the need for treatment at an early age, the prosthetic management of such a young child can be difficult. Complete dentures were provided to encourage a normal psychological development and to improve the function of the stomatognathic system.


2010 ◽  
Vol 49 (9) ◽  
pp. 1050-1055 ◽  
Author(s):  
Nayellin Reyes-Chicuellar ◽  
Roberto De Haro ◽  
Rafael Jiménez-Flores ◽  
Jovita Monje-Martínez ◽  
Norma Motta-Castañeda ◽  
...  

Author(s):  
Heba Alajami ◽  
Jamal Saker

Hypohidrotic ectodermal dysplasia is a heritable disease, characterized by hypodontia, hypotrichosis, and anhidrosis. This clinical report demonstrates prosthetic rehabilitation of a patient complaining of impaired mastication and the odd appearance of her jaws. Maxillary telescopic-overdenture and implant-supported mandibular prostheses were fabricated to improve mastication, speech, and aesthetics of the patient.


Author(s):  
Emilija Bajraktarova Valjakova ◽  
Cvetanka Misevska ◽  
Vesna Korunoska Stevkovska ◽  
Nikola Gigovski ◽  
Ana Sotirovska Ivkovska ◽  
...  

RSBO ◽  
2017 ◽  
Vol 14 (1) ◽  
pp. 44-09
Author(s):  
Mariana Dalledone ◽  
Fernanda Mara de Paiva Bertoli ◽  
Ana Paula Sponchiado ◽  
Estela Maris Losso ◽  
João Armando Brancher ◽  
...  

Ectodermal dysplasia is an abnormality of the ectoderm and its derivatives, phenotypically expressed in males and genetically inherited from mothers. Objective: To report the efficacy of the prosthetics treatment of severe ectodermal dysplasia in a 6-year-old boy with hypohidrotic ectodermal dysplasia (HED). Case report: The boy had difficulty in speaking and eating and the condition also affected his self-esteem. Prosthetic treatments included the construction of acrylic custom trays, determination of the vertical dimension of occlusion (VDO), construction of upper and lower dentures, and palatal expansion procedure. Conclusion: Significant improvements in the patient’s stomatognathic function and self-esteem were evident.


2020 ◽  
Vol 8 (3) ◽  
pp. 26
Author(s):  
Monireh Haghifar

Ectodermal dysplasia is a disease that affects components of body with ectodermal origin, so it is manifested by thin hair, malformed or missing teeth and lack of sweating. In this case, I present a 4 year old boy with hypohidrotic ectodermal dysplasia. He had psychological issues and difficulty in eating. In this young child, with prosthetic treatment that included partial removable denture, his problems was dissolved.


2021 ◽  
Vol 45 (6) ◽  
pp. 421-427
Author(s):  
Alix Maria Gregory Sawaya de Castro ◽  
Maria Salete Nahás Pires Corrêa ◽  
Fernanda Nahás Pires Corrêa ◽  
Cristiane de Almeida Baldini Cardoso ◽  
Stella Ferreira do Amaral ◽  
...  

Background: This case report presents the dimensional changes in dental arches in a patient with hypohidrotic ectodermal dysplasia (HED) after complete denture rehabilitation, with an 18-year follow-up period. Case report: The patient had complete anodontia and was successfully rehabilitated with conventional complete dentures at 3, 4, 5, 7, 9, 12, 16, and 21 years of age. Each successive denture was larger and contained more and larger teeth so as to accommodate for the increase in the size of the developing jaw. A series of diagnostic casts were used to measure the dimensional changes in the arch length and width of the alveolar ridge. Cast analysis revealed that there was an increase in arch length and width in both the maxilla and mandible over time. Cephalometric analysis of craniofacial development was performed at 21 years of age, and suggested protrusion of the maxilla and mandible. Conclusions: The absence of teeth due to HED did not affect the dimensional changes in dental arches after complete denture rehabilitation from childhood to adulthood. The prosthetic treatment improved the patient’s social integration and enabled the development of normal dietary habits, speech, and facial esthetics, which in turn led to improved quality of life.


2013 ◽  
Vol 11 (1) ◽  
pp. 39-42
Author(s):  
Mahya Sultan Tosun ◽  
Vildan Ertekin ◽  
Mustafa Buyukavci ◽  
Hakan Doneray

2010 ◽  
Vol 43 (01) ◽  
pp. 092-096
Author(s):  
Sanjeev N. Deshpande ◽  
Vikas Kumar

ABSTRACTEctodermal dysplasia is a rare group of inherited disorders characterized by aplasia or dysplasia of tissues of ectodermal origin, such as hair, nails, teeth and skin. Dental manifestations include hypodontia, complete anodontia or malformed teeth. Oral rehabilitation is the major surgical challenge in such patients. It frequently requires alveolar reconstruction followed by dental implants. We report a case of hypohidrotic ectodermal dysplasia, which was managed with reconstruction of both the upper and the lower alveolus using free fibula flaps with dental rehabilitation using osseointegrated implants.


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