Mahmood Syeda Hania, Khan Maria, Qadar Laila Tul, Yousuf Fareeha, Hasan Mohammad
Internal Medicine, Dow University of Health Sciences, Karachi, PAK.
Pediatrics, Dow University of Health Sciences, Karachi, PAK.
Cureus. 2019 Sep 21;11(9):e5717. doi: 10.7759/cureus.5717.
Bardet-Biedl syndrome (BBS) is a rare autosomal recessive genetic disorder. It is a congenital ciliopathy that has primary and secondary characteristics. Primary clinical features include rod-cone dystrophy, polydactyly, central obesity, genital abnormalities and mental retardation often presenting as learning difficulties. Secondary clinical features include developmental delay, speech deficit, brachydactyly/syndactyly, dental defects, ataxia, olfactory deficit, diabetes mellitus (DM) and congenital heart disease. BBS patients are friendly with a happy predisposition. Proper management, and regular examinations should be done in order to maintain healthy organ function and to avoid an early death. Renal failure is the most common cause of mortality in BBS patients.This case report illustrates the evaluation of a child with BBS, as well as the unique association of otolaryngologic symptoms and bronchopneumonia with it.
巴德-比德尔综合征(BBS)是一种罕见的常染色体隐性遗传病。它是一种先天性纤毛病,具有原发性和继发性特征。主要临床特征包括视锥视杆营养不良、多指畸形、中枢性肥胖、生殖器异常和智力发育迟缓,常表现为学习困难。次要临床特征包括发育迟缓、言语缺陷、短指/并指、牙齿缺陷、共济失调、嗅觉缺陷、糖尿病(DM)和先天性心脏病。BBS患者性格友善,天性乐观。应进行适当的管理和定期检查,以维持器官功能健康,避免过早死亡。肾衰竭是BBS患者最常见的死亡原因。本病例报告阐述了一名BBS患儿的评估情况,以及耳鼻喉科症状和支气管肺炎与之的独特关联。