Christ-Siemens-Touraine syndrome: A rare case report

Christ-Siemens-Touraine syndrome/hypohidrotic ectodermal dysplasia (HED) is a heterogeneous group of inherited disorders with primary defects in tissues derived from embryonic ectoderm such as hair, tooth, nail, and sweat glands. To date, more than 192 distinct disorders have been described. Here we...

Full description

Saved in:
Bibliographic Details
Published inJournal of pharmacy & bioallied science Vol. 11; no. 1; pp. 102 - 104
Main Authors Kumar, Anoop, Thomas, Priya, Muthu, Therraddi, Mathayoth, Maya
Format Journal Article
LanguageEnglish
Published India Wolters Kluwer India Pvt. Ltd 01.01.2019
Medknow Publications and Media Pvt. Ltd
Medknow Publications & Media Pvt. Ltd
Medknow Publications & Media Pvt Ltd
Wolters Kluwer Medknow Publications
Subjects
Care and treatment
Case Report
Case reports
Christ–Siemens–Touraine syndrome
Defects
Diagnosis
Dysplasia
Ectoderm
Ectodermal dysplasia
Embryos
Enamel
Females
Gene mutations
Hereditary diseases
hypodontia
hypohidrotic ectodermal dysplasia
Mutation
Prostheses
Signal transduction
Speech therapists
Sweat
Sweat gland
Teeth
Christ-Siemens-Touraine syndrome
hypodontia
hypohidrotic ectodermal dysplasia
Christ–Siemens–Touraine syndrome
Online AccessGet full text

Cover

More Information
Summary:Christ-Siemens-Touraine syndrome/hypohidrotic ectodermal dysplasia (HED) is a heterogeneous group of inherited disorders with primary defects in tissues derived from embryonic ectoderm such as hair, tooth, nail, and sweat glands. To date, more than 192 distinct disorders have been described. Here we present a case of 19-year-old female patient that manifested with HED (Christ-Siemens-Touraine syndrome).
ISSN:0975-7406
0976-4879
0975-7406
DOI:10.4103/JPBS.JPBS_36_18