Literature DB >> 20215674

Hypohidrotic ectodermal dysplasia - diagnostic aids and a report of 5 cases.

K Ramesh1, D Vinola, John B John.   

Abstract

Hypohidrotic ectodermal dysplasia (HED) is a rare group of disorders affecting the hair, teeth, nails and sweat glands to a variable degree. There is a wide range of clinical presentation of HED. Missing teeth or abnormal tooth form may be the first indicator of the disorder. We present a case report of 5 cases of HED with their intraoral findings and their treatment plan. We also consider the various etiological factors and their clinical diagnostic aids.

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Year:  2010        PMID： 20215674     DOI： 10.4103/0970-4388.60474

Source DB:  PubMed          Journal:  J Indian Soc Pedod Prev Dent        ISSN： 0970-4388


  11 in total

1.  Familial ectodermal dysplasia: a peers' agony.

Authors:  Karthik Hegde; Roopashri Rajesh Kashyap; Gopakumar Nair; Preeti P Nair
Journal:  BMJ Case Rep       Date:  2013-07-23

2.  Prosthodontic management of patients with Christ-Siemens-Touraine syndrome.

Authors:  Anand Shigli; Priyanka Airen Sarkar
Journal:  BMJ Case Rep       Date:  2012-06-28

3.  Evaluation of sweat production by pilocarpine iontophoresis: a noninvasive screening tool for hypohidrosis in ectodermal dysplasia.

Authors:  Surupa Basu; Monjori Mitra; Apurba Ghosh
Journal:  Indian J Clin Biochem       Date:  2013-05-15

4.  An unusual case of ectodermal dysplasia: combating senile features at an early age.

Authors:  Mudit Gupta; Kumbar Jayadevappa Sundaresh; Manu Batra; Vandana J Rathva
Journal:  BMJ Case Rep       Date:  2014-02-03

5.  Conservation analysis and pathogenicity prediction of mutant genes of ectodysplasin a.

Authors:  Fangqi He; Hongfeng Wang; Xiaoyu Zhang; Qingping Gao; Feng Guo; Chang Chen
Journal:  BMC Med Genet       Date:  2018-12-07       Impact factor: 2.103

6.  Self-Assessment of Oral Health-Related Quality of Life in People with Ectodermal Dysplasia in Germany.

Authors:  Marcel Hanisch; Sonja Sielker; Susanne Jung; Johannes Kleinheinz; Lauren Bohner
Journal:  Int J Environ Res Public Health       Date:  2019-05-31       Impact factor: 3.390

7.  A novel frameshift mutation in the EDA gene in an Iranian patient affected by X-linked hypohidrotic ectodermal dysplasia.

Authors:  Marzieh Rahbaran; Maryam Hassani Doabsari; Simindokht Salavitabar; Neda Mokhberian; Ziba Morovvati; Saeid Morovvati
Journal:  Cell Mol Biol Lett       Date:  2019-08-19       Impact factor: 5.787

8.  [Anhydrotic ectodermal dysplasia associated to mannose-binding lectin deficiency].

Authors:  I Delgado Pecellín; Y Castillo Reguera; C Delgado Pecellín; M A Bueno Delgado; J P González Valencia; I Obando Santaella; O Neth
Journal:  An Pediatr (Barc)       Date:  2012-04-01       Impact factor: 1.500

9.  First report of X-linked hypohidrotic ectodermal dysplasia with a hemizygous c.1142G > C in the EDA gene: variant of uncertain significance or new pathogenic variant?

Authors:  Mario Tumminello; Antonella Gangemi; Federico Matina; Melania Guardino; Bianca Lea Giuffrè; Giovanni Corsello
Journal:  Ital J Pediatr       Date:  2021-06-02       Impact factor: 2.638

10.  Telescopic overdenture for oral rehabilitation of ectodermal dysplasia patient.

Authors:  Charu Gupta; Mahesh Verma; Rekha Gupta; Shubhra Gill
Journal:  Contemp Clin Dent       Date:  2015-09
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