Anhidrotic ectodermal dysplasia in an adolescent boy: Case report and review of literature

2021 ◽  
Vol 17 (2) ◽  
pp. 74
Author(s):  
Thirunavukkarasu Arun Babu ◽  
Padmapriya Balakrishnan
Keyword(s):  
Case Report ◽  
Ectodermal Dysplasia ◽  
Review Of Literature ◽  
Anhidrotic Ectodermal Dysplasia

scholarly journals An infant with X‐linked anhidrotic ectodermal dysplasia with immunodeficiency presenting with Pneumocystis pneumonia: A case report

2021 ◽  
Vol 9 (11) ◽  
Author(s):  
Miwako Toyohara ◽  
Yuko Kajiho ◽  
Etsushi Toyofuku ◽  
Chie Takahashi ◽  
Keiho Owada ◽  
...  
Keyword(s):  
Case Report ◽  
Ectodermal Dysplasia ◽  
Pneumocystis Pneumonia ◽  
Anhidrotic Ectodermal Dysplasia

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.

scholarly journals CASE REPORT OF ANHIDROTIC ECTODERMAL DYSPLASIA (CHRIST - SEIMENS - TOURAINE SYNDROME)

2013 ◽  
Vol 2 (49) ◽  
pp. 9441-9443
Author(s):  
Gopal M.G ◽  
Sreedevi Chandrika M ◽  
Sharath Kumar B.C ◽  
Ramesh M ◽  
Nandini A.S
Keyword(s):  
Case Report ◽  
Ectodermal Dysplasia ◽  
Anhidrotic Ectodermal Dysplasia

scholarly journals Surgical resection of an infectious pulmonary cyst in a patient with anhidrotic ectodermal dysplasia: A case report

2020 ◽  
Vol 34 (4) ◽  
pp. 275-280
Author(s):  
Raito Maruyama ◽  
Keigo Matsushima ◽  
Masashi Mikubo ◽  
Yoshio Matsui ◽  
Kazu Shiomi ◽  
...  
Keyword(s):  
Case Report ◽  
Surgical Resection ◽  
Ectodermal Dysplasia ◽  
Anhidrotic Ectodermal Dysplasia ◽  
Pulmonary Cyst

scholarly journals Ectodermal Dysplasia Presenting with Atrophic Rhinitis: Report of Two Cases and Review of Literature

2015 ◽  
Vol 8 (3) ◽  
pp. 133-135 ◽  
Author(s):  
Sampurna Pati ◽  
Sudipta Pal ◽  
Somnath Saha ◽  
Surajit Biswas
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Conservative Therapy ◽  
Ectodermal Dysplasia ◽  
Tertiary Care ◽  
Atrophic Rhinitis ◽  
Mucosal Biopsy ◽  
Review Of Literature ◽  
History Of ◽  
Conventional Manner

ABSTRACT Aim To present two rare case of ectodermal dysplasia presenting with maggot infestation due to atrophic rhinitis. Study design Case report. Setting Tertiary care referral hospital. Presentation Two male child aged about 5 and 8 years presented in ENT emergency with history of maggot infestation of nose. Result Clinical examination was suggestive of ectodermal dysplasia. Intranasal examination was suggestive of atrophic rhinitis. Maggots were removed in conventional manner. Following conservative treatment, skin biopsy and nasal mucosal biopsy was taken which confirmed the diagnosis of ectodermal dysplasia. Conclusion Any ectodermal dysplasia patient should be suspected of having atrophic rhinitis and intranasal conservative therapy should be initiated at the earliest to prevent complication like maggots in nose. How to cite this article Pati S, Pal S, Saha S, Biswas S. Ectodermal Dysplasia Presenting with Atrophic Rhinitis: Report of Two Cases and Review of Literature. Clin Rhinol An Int J 2015;8(3):133-135.

scholarly journals Prosthetic dental management of a patient with anhidrotic ectodermal dysplasia. A Case Report.

2021 ◽  
Vol 10 (4) ◽  
pp. 1-6
Author(s):  
Daniel Hernández-González ◽  
◽  
Jennifer Orozco-Páez ◽  
Keyword(s):  
Case Report ◽  
Multidisciplinary Approach ◽  
Ectodermal Dysplasia ◽  
Genetic Disorders ◽  
Stomatognathic System ◽  
Lower Jaw ◽  
Correct Analysis ◽  
Dental Management ◽  
Cad Cam ◽  
Anhidrotic Ectodermal Dysplasia

Introduction: Ectodermal dysplasia (ED) comprises a broad group of genetic disorders characterized by alterations of the structures derived from the ectoderm, including those of the stomatognathic system. Case Report: The present article aims to report the prosthetic management of a patient with anhidrotic ectodermal dysplasia. A male patient diagnosed with ED who attended the dental consultation displaying oligodontia; underdeveloped alveolar ridges were observed. Results: The established treatment consisted of the adaptation of implant-supported fixed full-arch prosthesis designed through CAD-CAM technology for the lower jaw and of a removable partial prosthesis with muco-dental support for the upper jaw. The dental approach of patients with ED is based on a correct analysis of the facial characteristics and stomatological conditions of each subject. Conclusion: A multidisciplinary approach is mandatory due to the biological and functional complexity in biomechanical terms of these individuals.

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