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...

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Príomhchruthaitheoirí: Anoop Kumar (Údar), Priya Thomas (Údar), Therraddi Muthu (Údar), Maya Mathayoth (Údar)
Formáid: LEABHAR
Foilsithe / Cruthaithe: Wolters Kluwer Medknow Publications, 2019-01-01T00:00:00Z.
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100 1 0 |a Anoop Kumar  |e author 
700 1 0 |a Priya Thomas  |e author 
700 1 0 |a Therraddi Muthu  |e author 
700 1 0 |a Maya Mathayoth  |e author 
245 0 0 |a Christ-Siemens-Touraine syndrome: A rare case report 
260 |b Wolters Kluwer Medknow Publications,   |c 2019-01-01T00:00:00Z. 
500 |a 0975-7406 
500 |a 10.4103/JPBS.JPBS_36_18 
520 |a 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). 
546 |a EN 
690 |a Christ-Siemens-Touraine syndrome 
690 |a hypodontia 
690 |a hypohidrotic ectodermal dysplasia 
690 |a Pharmacy and materia medica 
690 |a RS1-441 
690 |a Analytical chemistry 
690 |a QD71-142 
655 7 |a article  |2 local 
786 0 |n Journal of Pharmacy and Bioallied Sciences, Vol 11, Iss 1, Pp 102-104 (2019) 
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