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| CASE REPORT |
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| Year : 2022 |
Volume
: 26 | Issue : 5 | Page
: 12-16 |
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Hypohidrotic ectodermal dysplasia: A case report with review and latest updates
Shubhangi P Bagdey, Rohit B Moharil, Alka Dive, Ashish Bodhade
Department of Oral Pathology, VSPMDCRC, Nagpur, Maharashtra, India
Correspondence Address:
Shubhangi P Bagdey
Department of Oral Pathology, VSPMDCRC, Digdoh Hills, Nagpur, Maharashtra
India
 Source of Support: None, Conflict of Interest: None  | Check |
DOI: 10.4103/jomfp.jomfp_287_21
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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.
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