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Hypohidrotic ectodermal dysplasia with autosomal recessive inheritance pattern: Report of a rare and unusual case with a brief review of literature
| Content Provider | Scilit |
|---|---|
| Author | Sawai, MadhuriAlankar Hasan, Shamimul Govind, Murali Ansari, MohammadDilshad |
| Copyright Year | 2019 |
| Abstract | Ectodermal dysplasia (ED) is a congenital disorder primarily affecting the ectodermal tissue, with infrequent dysfunction of mesodermally derived tissues. Clinically, there are two major forms seen, hypohidrotic/Christ–Siemens–Touraine syndrome and hidrotic/Clouston syndrome, depending on the number and function of sweat glands. A multidisciplinary treatment protocol is usually followed and necessitates collective efforts by medical and dental professionals. Dental intervention should be done as early as possible to ameliorate the patient's esthetics and enhance the emotional and psychological quotient in these patients. This case report aims to highlight a rare and interesting report of hypohidrotic ED in a young female patient with a possible autosomal recessive inheritance pattern. |
| Related Links | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6948050/pdf |
| Ending Page | 479 |
| Page Count | 1 |
| Starting Page | 479 |
| File Format | XHTML |
| ISSN | 0973029X |
| e-ISSN | 1998393X |
| DOI | 10.4103/jomfp.JOMFP_98_19 |
| Journal | Journal of Oral and Maxillofacial Pathology |
| Issue Number | 3 |
| Volume Number | 23 |
| Language | English |
| Publisher | Medknow |
| Access Restriction | Open |
| Subject Keyword | Dermatology Autosomal Recessive Christ–siemens–touraine Syndrome Ectodermal Dysplasia Hypohidrosis Hypotrichosis Oligodontia Journal of Oral and Maxillofacial Pathology, Volume 23, Issue 3 |
| Content Type | Text |
| Resource Type | Article |
| Subject | Dentistry Otorhinolaryngology Pathology and Forensic Medicine |
