Christ Siemen Syndrome - a Report of Two Cases

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Authors

  • Koteeswaran D.
     ,IN
  • Choudary A. S.
     ,IN
  • Gopal K. S.
     ,IN
  • Ramani P.
     ,IN

Keywords:

Ectodermal Dysplasia, Christ -Siemens Tourine Syndrome, Anodontia, Hypohydrosis, Hypotrichosis, Clustons Syndrome

Abstract

Ectodermal Dysplasia (ED) is a rare hereditary disorder which is characterized by triad of signs comprising sparse hair, abnormal or missing teeth and inability to sweat. This article comprises of 2 such cases one of a 5 year old child with hypohydroic ectodermal dysplasia and a 15 year old female patient of clustons syndrome. This paper also highlights about history, clinical features, differential diagnosis and treatment options of such patients.

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Published

2011-09-01

How to Cite

D., K., A. S., C., K. S., G., & P., R. (2011). Christ Siemen Syndrome - a Report of Two Cases. Journal of Pierre Fauchard Academy (India Section), 25(3), 172–176. Retrieved from https://informaticsjournals.com/index.php/jpfa/article/view/23060

Issue

Volume 25, Issue 3, September 2011

Section

Original Articles

License

All the articles published in JPFA are distributed under a creative commons license. The journal allows the author(s) to hold the copyright of their work (all usages allowed except for commercial purpose).