一名患有斯蒂克勒综合征婴儿的喂养困难

Vijay Parvathy, Kumaran Parvathy, Xavier Arun Mamachan, Varma R Balagopal, Kumar J Suresh

Department of Pedodontics and Preventive Dentistry, Amrita School of Dentistry, Amrita Institute of Medical Sciences, Amrita University, Kochi, Kerala, India.

Contemp Clin Dent. 2019 Jul-Sep;10(3):558-560. doi: 10.4103/ccd.ccd_749_18.

Stickler syndrome or hereditary progressive arthro-ophthalmopathy is an autosomal dominant condition characterized by ocular manifestations, arthritic changes, orofacial features, and deafness, in variable degrees. This is a case report of a 48-day-old infant who presented with severe feeding difficulty. It also details the clinical, diagnostic features, and management of an infant with Stickler syndrome.

斯蒂克勒综合征或遗传性进行性关节眼病是一种常染色体显性疾病，其特征为不同程度的眼部表现、关节炎变化、口面部特征和耳聋。本文报告了一名48日龄婴儿，该婴儿出现严重喂养困难。本文还详细介绍了一名患有斯蒂克勒综合征婴儿的临床、诊断特征及治疗情况。