Hypohidrotic ectodermal dysplasia: A case report with review and latest updates.
| Autor: | Bagdey SP; Department of Oral Pathology, VSPMDCRC, Nagpur, Maharashtra, India., Moharil RB; Department of Oral Pathology, VSPMDCRC, Nagpur, Maharashtra, India., Dive A; Department of Oral Pathology, VSPMDCRC, Nagpur, Maharashtra, India., Bodhade A; Department of Oral Pathology, VSPMDCRC, Nagpur, Maharashtra, India. |
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| Jazyk: | angličtina |
| Zdroj: | Journal of oral and maxillofacial pathology : JOMFP [J Oral Maxillofac Pathol] 2022 Feb; Vol. 26 (Suppl 1), pp. S12-S16. Date of Electronic Publication: 2022 Feb 28. |
| DOI: | 10.4103/jomfp.jomfp_287_21 |
| Abstrakt: | Ectodermal dysplasia represents a group of inherited conditions in which two or more ectodermally derived anatomical structures fail to develop resulting in most notably anhidrosis/hypohidrosis, hypotrichosis and hypodontia. It is a xlinked recessive disorder with male predominance. We report a classical case in a 17-year-old male with emphasis on review of literature and latest updates. Competing Interests: There are no conflicts of interest. (Copyright: © 2022 Journal of Oral and Maxillofacial Pathology.) |
| Databáze: | MEDLINE |
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