| Literature DB >> 32641302 |
Nitesh Tewari1, Vijay Prakash Mathur1, Rigzin Tamchos1, Morankar Rahul2.
Abstract
Lamellar ichthyosis (LI) is a rare genetic condition that affects the skin, with an incidence of less than 1:300 000 in different parts of the world. This report describes a case of a 5-year-old girl with LI and rickets presenting with premature loss of 51, 52, 61, 62 and 71, grade II mobility in 72, 73, 81, 82 and 83 along with loss of supporting bone with 53, 63, 72, 73, 82 and 83. This is the first report describing oral manifestations of this combination of LI and rickets. © BMJ Publishing Group Limited 2020. No commercial re-use. See rights and permissions. Published by BMJ.Entities:
Keywords: congenital disorders; dentistry and oral medicine; dermatology; mouth
Mesh:
Year: 2020 PMID: 32641302 PMCID: PMC7348650 DOI: 10.1136/bcr-2020-235008
Source DB: PubMed Journal: BMJ Case Rep ISSN: 1757-790X