Hypohidrotic hereditary ectodermal dysplasia: A case report

Author:

Sachdev Sanpreet Singh,Padawe Dimple1,Khade Ankita2,Takate Vilas,Dighe Kishore

Affiliation:

1. Government Dental College and Hospital, Mumbai, Maharashtra, India

2. o

Abstract

Hypohidrotic Ectodermal Dysplasia (HED) is characterized by a triad of hypotrichosis (sparse hair), hypodontia (multiple missing teeth), and hypohidrosis (inability to sweat adequately). Consequently, patients’ quality of life is severely affected due to impairments in mastication, speech, and esthetics. Timely oral rehabilitation of patients with HED can enable them to lead a normal life by helping them perform their functions adequately and prevent the psychological ill-effects; in which dental professionals play a key role. The present case report describes the oral rehabilitation and management of a 7-year-old male patient with HED.

Publisher

IP Innovative Publication Pvt Ltd

Subject

Microbiology

Reference11 articles.

1. Ectodermal dysplasias: Clinical and molecular review

2. Cluzeau C, Hadj-Rabia S, Jambou M, Mansour S, Guigue P, Masmoudi S, Only four genes (EDA1, EDAR, EDARADD, and WNT10A) account for 90% of hypohidrotic/anhidrotic ectodermal dysplasia cases.Hum Mutat 2011;32(1):70-2

3. Ectodermal Dysplasia: A Genetic Review

4. Paramkusam G, Meduri V, Nadendla L K, Shetty N, Hereditary hypohidrotic ectodermal dysplasia: report of a rare case.J Clin Diagn Res 2013;7(9):2074-5

5. Kumar V, Kumar L, Hereditary Ectodermal Dysplasia: A Case Report.J Indian Soc Pedod Prev Dent 2015;2(3):54-8

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