Hereditary Ectodermal Dysplasia in the U. S. Navy: Case Report

1966 ◽  
Vol 131 (9) ◽  
pp. 819-822
Author(s):  
James W. Reid
Keyword(s):  
Case Report ◽  
Ectodermal Dysplasia

Ectodermal Dysplasia in two siblings: A Case report.

2019 ◽  
Author(s):  
CHAITHRA KALKUR ◽  
NILOFER HALIM ◽  
ANUSHA RANGARE ◽  
Rumisha .
Keyword(s):  
Case Report ◽  
Key Words ◽  
Clinical Features ◽  
Ectodermal Dysplasia ◽  
Heterogeneous Group ◽  
Eccrine Glands ◽  
Key Words Ectodermal Dysplasia

Ectodermal dysplasia is a heterogeneous group of inherited disorder affecting two or more ectodermally derived tissues such as skin, hair, nails, eccrine glands and teeth. The disorder is of two types: Hypohydrotic ectodermal dysplasia/Christ seimens –Touraine syndrome and Hydrotic ectodermal dysplasia/clousten syndrome. Commonly associated signs include hypohidrosis, anomalous dentition, onychodysplasia, hypotrichosis. Multidisciplinary approaches are required for optimal treatment3. Here, we present two cases of 19 and 13 year old male siblings who were diagnosed with the disorder based upon their clinical features. Key Words: ectodermal dysplasia, hypodontia; anomalous dentition.

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 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

Ectodermal dysplasia with anodontia – case report

2016 ◽  
Vol 69 (3) ◽  
pp. 374-378
Author(s):  
Jerzy Błaszczak ◽  
Agnieszka Skawińska ◽  
Maria Mielnik-Błaszczak
Keyword(s):  
Case Report ◽  
Ectodermal Dysplasia

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.

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