scholarly journals Ectodermal dysplasia - Maxillary and mandibular alveolar reconstruction with dental rehabilitation: A case report and review of the literature

2010 ◽  
Vol 43 (01) ◽  
pp. 092-096
Author(s):  
Sanjeev N. Deshpande ◽  
Vikas Kumar
Keyword(s):  
Case Report ◽  
Ectodermal Dysplasia ◽  
Review Of The Literature ◽  
Hypohidrotic Ectodermal Dysplasia ◽  
Inherited Disorders ◽  
Oral Rehabilitation ◽  
Osseointegrated Implants ◽  
Dental Rehabilitation ◽  
Free Fibula ◽  
Rare Group

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.

scholarly journals EDA mutation as a cause of hypohidrotic ectodermal dysplasia: a case report and review of the literature

2015 ◽  
Vol 14 (3) ◽  
pp. 10344-10351 ◽  
Author(s):  
S.X. Huang ◽  
J.L. Liang ◽  
W.G. Sui ◽  
H. Lin ◽  
W. Xue ◽  
...  
Keyword(s):  
Case Report ◽  
Ectodermal Dysplasia ◽  
Review Of The Literature ◽  
Hypohidrotic Ectodermal Dysplasia

scholarly journals Oral rehabilitation with removable dental prosthesis in a six-year-old patient with hypohidrotic ectodermal dysplasia

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 ◽  
...  
Keyword(s):  
Case Report ◽  
Ectodermal Dysplasia ◽  
Self Esteem ◽  
Vertical Dimension ◽  
Hypohidrotic Ectodermal Dysplasia ◽  
Oral Rehabilitation ◽  
Palatal Expansion ◽  
Expansion Procedure ◽  
Removable Dental Prosthesis

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.

Treatment Considerations for a Patient with Hypohidrotic Ectodermal Dysplasia: A Case Report

2008 ◽  
Vol 9 (3) ◽  
pp. 128-134 ◽  
Author(s):  
Dilek Tüfekcioğlu ◽  
Chenkhan Bal ◽  
Bilge Turhan Bal
Keyword(s):  
Case Report ◽  
Behavioral Problems ◽  
Ectodermal Dysplasia ◽  
Young Patients ◽  
Hair Follicles ◽  
Sweat Glands ◽  
Clinical Report ◽  
Hypohidrotic Ectodermal Dysplasia ◽  
Oral Rehabilitation ◽  
Treatment Considerations

Abstract Aim This clinical report describes the oral rehabilitation of a 6-year-old male ectodermal dysplasia (ED) patient diagnosed with hypodontia. Background ED is a hereditary disease characterized by a congenital dysplasia of one or more ectodermal structures and their accessory appendages. Common manifestations include defective hair follicles and eyebrows, frontal bossing with prominent supraorbital ridges, nasal bridge depression, and protuberant lips. Intraorally, most common findings are anadontia or hypodontia, conical teeth, and generalize spaces. The patient may suffer from dry skin, hyperthermia, and unexplained high fever as a result of deficiency of sweat glands. Report A six-year-old boy who exhibited many of the manifestations of ED as well as behavioral problems and a severe gag reflex. The treatment was designed to improve his appearance and oral functions and included the fabrication of several removable prostheses and acid-etched composite resin restorations during his growth and development. Summary Young patients with ED need to be evaluated early by a dental professional to determine the oral ramifications of the condition. When indicated, appropriate care needs to be rendered throughout the child's growth cycle to maintain oral functions as well as to address the esthetic needs of the patient. This clinical report demonstrates that removable partial dentures associated with direct composite restorations can be a reversible and inexpensive method of treatment for young ED patients. Citation Bal C, Bal BT, Casela L, Tüfekçioğlu D. Treatment Considerations for a Patient with Hypohidrotic Ectodermal Dysplasia: A Case Report. J Contemp Dent Pract 2008 March; (9)3:128-134.

scholarly journals Oral rehabilitation with removable dental prosthesis in a six-year-old patient with hypohidrotic ectodermal dysplasia

RSBO ◽  
2017 ◽  
Vol 1 (1) ◽  
pp. 44
Author(s):  
Mariana Dalledone ◽  
Fernanda Mara De Paiva Bertoli ◽  
Ana Paula Sponchiado ◽  
Estela Maris Losso ◽  
João Armando Brancher ◽  
...  
Keyword(s):  
Case Report ◽  
Ectodermal Dysplasia ◽  
Self Esteem ◽  
Vertical Dimension ◽  
Hypohidrotic Ectodermal Dysplasia ◽  
Oral Rehabilitation ◽  
Palatal Expansion ◽  
Expansion Procedure ◽  
Removable Dental Prosthesis

Introduction: 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 functionand self-esteem were evident.

scholarly journals Atrophic jaw fracture and predictability in oral rehabilitation: case report

2020 ◽  
Vol 23 (3) ◽  
Author(s):  
João Pedro Miola Siqueira de Oliveira ◽  
Paola Fernanda Cotait de Lucas Corso ◽  
Gilson Cristiano De Oliveira ◽  
Rafaela Scariot ◽  
Davani Latarullo Costa
Keyword(s):  
Case Report ◽  
Dental Implants ◽  
Correct Diagnosis ◽  
Functional Results ◽  
Normal Function ◽  
Oral Rehabilitation ◽  
Osseointegrated Implants ◽  
Fixation Techniques ◽  
Mandibular Body ◽  
Jaw Fractures

Introduction: The treatment of atrophic jaw fractures requires extensive knowledge by the maxillofacial surgeon. The correct diagnosis and planning optimize the possibility of oral rehabilitation towards many possible alternatives. The difficulty in repairing these fractures makes the treatment complex, in which normally invasive techniques are used. However; which give us satisfactory and predictable aesthetic-functional results. Objective: The objective of this work is to report an atrophic jaw fracture and posterior dental implants rehabilitation. Case report: A 53 years old female patient, victim of in face aggression referred to the emergency care. At the clinical examination, the patient had laceration in the upper lip region and the left side of the mandibular area, with bilateral mobility and paresis. In the oral examination, total lower and partial upper edentulism. After tomographic evaluation, a bilateral fracture of the mandibular body was confirmed, with significant bone fragments uneven. Surgery was performed with total transcervical access and use of reconstruction plate. After 90 days of follow-up, the oral rehabilitation with osseointegrated implants was performed. Conclusion: Complex atrophic mandible fractures in total edentulous patients can be treated with open reduction and stable fixation, allowing a faster return to normal function, improve of quality of life and assists in increasing safety for implant installation.KeywordsEdentulous jaw; Jaw fixation techniques; Dental implants.

Hypohidrotic ectodermal dysplasia: dental, clinical, genetic and dermatoglyphic findings of three cases

2002 ◽  
Vol 26 (1) ◽  
pp. 5-12 ◽  
Author(s):  
B. Kargül ◽  
T. Alcan ◽  
U. Kabalay ◽  
M. Atasu
Keyword(s):  
Ectodermal Dysplasia ◽  
Oral Surgery ◽  
Clinical Manifestations ◽  
Pediatric Dentistry ◽  
Permanent Teeth ◽  
Maxillofacial Radiology ◽  
Hypohidrotic Ectodermal Dysplasia ◽  
Clinical Genetic ◽  
Osseointegrated Implants ◽  
Removable Prosthesis

Patients with hypohidrotic ectodermal dysplasia (HED) are characterized by the clinical manifestations of hypodontia, hypohidrosis, hypotrichosis and a highly characteristic facial physiognomy. This disorder is inherited as an X- linked trait. This report presents three cases with HED in which the clinical evaluation (intraoral and radiological), genetic findings and SEM examination of hair. Boys 6 to 14 year old and a 11 year old girl were referred to the Marmara University, Faculty of Dentistry, complaining of oligodontia in the maxillary and mandibular arches and delay in eruption of other teeth. Peg-shaped teeth have been observed. The dermatoglyphs of the patients were striking. SEM exmimation of hair demostrated a distinctly abnormal longitudinal groving along the entire length of each hair and a desquamation of the surface cuticles. The treatment was planned in a multidisciplinary odontological group involving pediatric dentistry, orthodontics, prosthodontics and oral surgery and maxillofacial radiology of future dental habilitation. A specially designed overdenture, a removable prosthesis and osseointegrated implants were constructed. Periodic recall visits were advised, to monitor the dentures and implants during periods of growth and development, and eruption of the permanent teeth.

Clinical management of hypohidrotic ectodermal dysplasia with anodontia: case report

2003 ◽  
Vol 27 (1) ◽  
pp. 5-8 ◽  
Author(s):  
Ekaterini Paschos ◽  
Karin Christine Huth ◽  
Reinhard Hickel
Keyword(s):  
Case Report ◽  
Young Child ◽  
Clinical Management ◽  
Ectodermal Dysplasia ◽  
Psychological Development ◽  
Early Age ◽  
Complete Dentures ◽  
Hypohidrotic Ectodermal Dysplasia ◽  
Need For Treatment ◽  
Stomatognathic System

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.

scholarly journals Christ-Siemens-Touraine Syndrome: A Case Report and Review of the Literature

2012 ◽  
Vol 2012 ◽  
pp. 1-3 ◽  
Author(s):  
Sepideh Mokhtari ◽  
Saeedeh Mokhtari ◽  
Ali Lotfi
Keyword(s):  
Case Report ◽  
Ectodermal Dysplasia ◽  
Classical Case ◽  
Common Type ◽  
Rare Disorder ◽  
Review Of The Literature ◽  
Sebaceous Glands ◽  
Dental Abnormalities ◽  
Anhidrotic Ectodermal Dysplasia

Ectodermal dysplasia is a rare disorder with defects in two or more of the following structures: the teeth and the skin and its appendages including hair, nails, eccrine, and sebaceous glands. Anhidrotic ectodermal dysplasia is the most common type of disease. This rare disorder, also known as Christ-Siemens-Touraine syndrome, manifests as a triad of hypotrichosis, asteatosis, and anhidrosis. In view of the rarity of this entity, a classical case of anhidrotic ectodermal dysplasia is reported. We have also provided a review of recent investigations in the area of dental abnormalities in this syndrome.

Case report: Higher-than-expected prevalence of hypohidrotic ectodermal dysplasia in a rural Mexican setting: report of 20 cases

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