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Familial ectodermal dysplasia: a peers' agony.
BMJ Case Rep. 2013 Jul 23; 2013BC

Abstract

Ectodermal dysplasias include a various group of inherited disorders which share primary defect in the development of two or more tissues of embryonic ectodermal origin. Though there are many subtypes, ectodermal dysplasias are mainly hidrotic ectodermal dysplasia and hypohidrotic ectodermal dysplasia, among which the most common variety is X linked hypohidrotic ectodermal dysplasia. We report a rare case of X linked hypohidrotic ectodermal dysplasia occurring in a family with various skin, hair and oral abnormalities.

Authors+Show Affiliations

Department of Oral Medicine and Radiology, People's College of Dental Sciences and Research Centre, Bhopal, Madhya Pradesh, India.No affiliation info availableNo affiliation info availableNo affiliation info available

Pub Type(s)

Case Reports
Journal Article

Language

eng

PubMed ID

23880572

Citation

Hegde, Karthik, et al. "Familial Ectodermal Dysplasia: a Peers' Agony." BMJ Case Reports, vol. 2013, 2013.
Hegde K, Kashyap RR, Nair G, et al. Familial ectodermal dysplasia: a peers' agony. BMJ Case Rep. 2013;2013.
Hegde, K., Kashyap, R. R., Nair, G., & Nair, P. P. (2013). Familial ectodermal dysplasia: a peers' agony. BMJ Case Reports, 2013. https://doi.org/10.1136/bcr-2013-200175
Hegde K, et al. Familial Ectodermal Dysplasia: a Peers' Agony. BMJ Case Rep. 2013 Jul 23;2013 PubMed PMID: 23880572.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Familial ectodermal dysplasia: a peers' agony. AU - Hegde,Karthik, AU - Kashyap,Roopashri Rajesh, AU - Nair,Gopakumar, AU - Nair,Preeti P, Y1 - 2013/07/23/ PY - 2013/7/25/entrez PY - 2013/7/25/pubmed PY - 2014/10/21/medline JF - BMJ case reports JO - BMJ Case Rep VL - 2013 N2 - Ectodermal dysplasias include a various group of inherited disorders which share primary defect in the development of two or more tissues of embryonic ectodermal origin. Though there are many subtypes, ectodermal dysplasias are mainly hidrotic ectodermal dysplasia and hypohidrotic ectodermal dysplasia, among which the most common variety is X linked hypohidrotic ectodermal dysplasia. We report a rare case of X linked hypohidrotic ectodermal dysplasia occurring in a family with various skin, hair and oral abnormalities. SN - 1757-790X UR - https://www.unboundmedicine.com/medline/citation/23880572/Familial_ectodermal_dysplasia:_a_peers'_agony_ L2 - https://casereports.bmj.com/lookup/pmidlookup?view=long&pmid=23880572 DB - PRIME DP - Unbound Medicine ER -