Centre for Dental Education and Research, AIIMS, New Delhi, India.
Centre for Dental Education and Research, AIIMS, New Delhi, India
BMJ Case Rep. 2020 Jul 8;13(7):e235008. doi: 10.1136/bcr-2020-235008.
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.
板层状鱼鳞癣（LI）是一种罕见的遗传性疾病，影响皮肤，在世界不同地区的发病率低于 1/300000。本报告描述了一例 5 岁女孩患有 LI 和佝偻病，表现为 72、73、81、82 和 83 级 II 度活动度过早丧失，72、73、81、82 和 83 伴有 53、63、72、73、82 和 83 处支撑骨丧失。这是描述 LI 和佝偻病这一组合的口腔表现的首例报告。
