先天性失智伴短指畸形伴新型单侧先天性舌下神经麻痹和鹿角形肾结石

IF 0.2 Q4 DERMATOLOGY Indian Journal of Paediatric Dermatology Pub Date : 2022-10-01 DOI:10.4103/ijpd.ijpd_125_21
Anita Marak, Ellis Khawbung, Shakeel Jabbar, B. Shakthi
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引用次数: 0

摘要

先天性无甲症是一种相对罕见的指甲发育异常,影响所有或部分手指和脚趾指甲,其特征是指甲完全缺失或指甲发育不全。我们报告了一例罕见的先天性失智伴短指畸形,伴有独特的先天性心型舌异常、先天性舌下神经麻痹和鹿角结石。据我们所知,这些关联以前从未被描述过,也不属于任何已知的综合征实体。
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Congenital anonychia with brachydactyly with novel, unilateral congenital hypoglossal nerve palsy and staghorn renal calculus
Congenital anonychia is a relatively rare abnormality of nail development affecting all or some of the finger and toe nails, characterized by either complete absence of nails or hypoplasia of nails. We report a rare case of congenital anonychia with brachydactyly with unique congenital abnormalities of heart-shaped tongue, congenital hypoglossal nerve palsy, and staghorn calculus. To our knowledge, these associations have never been described before and do not fall under any known syndromic entity.
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0.00%
发文量
27
审稿时长
25 weeks
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