Suppr超能文献

Bardet Biedl Syndrome - A Report of Two Cases with Otolaryngologic Symptoms.

作者信息

Singh Mahendra K, Pradhan Sidharth, Chakraborty Priyanko

机构信息

Professor and Head, Department of Ophthalmology, Institute of Medical Sciences, BHU, Varanasi, Uttar Pradesh, India.

Junior Resident, Department of Ophthalmology, Institute of Medical Sciences, BHU, Varanasi, Uttar Pradesh, India.

出版信息

J Clin Diagn Res. 2017 Mar;11(3):ND01-ND02. doi: 10.7860/JCDR/2017/24499.9466. Epub 2017 Mar 1.

Abstract

Bardet-Biedl Syndrome (BBS) is a rare autosomal recessive disorder characterized primarily by rod-cone dystrophy, postaxial polydactyly, central obesity, mental retardation, hypogonadism, and renal dysfunction. We present two cases of this syndrome, both female, who presented with complaints of nyctalopia and mental retardation, and additionally one of them had sensorineural hearing loss while the other had serous otitis media. Hearing loss being a rare presentation is worth reporting. Both the patients were given a course of vitamin A and the parents were counseled regarding the prognosis and additional complications associated with the syndrome.

摘要

相似文献

1
Bardet Biedl Syndrome - A Report of Two Cases with Otolaryngologic Symptoms.
J Clin Diagn Res. 2017 Mar;11(3):ND01-ND02. doi: 10.7860/JCDR/2017/24499.9466. Epub 2017 Mar 1.
3
Bardet-Biedl syndrome with syndrome X: a patient report.
J Pediatr Endocrinol Metab. 2004 Jun;17(6):913-5. doi: 10.1515/jpem.2004.17.6.914.
4
Bardet-Biedl syndrome presenting with steroid sensitive nephrotic syndrome.
Indian J Nephrol. 2015 Sep-Oct;25(5):300-2. doi: 10.4103/0971-4065.151765.
6
A novel compound heterozygous mutation in identified in a Japanese patient.
Hum Genome Var. 2019 Mar 12;6:14. doi: 10.1038/s41439-019-0045-y. eCollection 2019.
7
A case of Bardet-Biedl syndrome complicated with intracranial hypertension in a Japanese child.
Brain Dev. 2014 Sep;36(8):721-4. doi: 10.1016/j.braindev.2013.10.013. Epub 2013 Nov 26.
8
Ciliopathy: Bardet-Biedl Syndrome.
Adv Exp Med Biol. 2018;1085:171-174. doi: 10.1007/978-3-319-95046-4_33.
9
Association of bifid epiglottis and laryngeal web with Bardet-Biedl syndrome: A case report.
Int J Pediatr Otorhinolaryngol. 2019 Jul;122:138-140. doi: 10.1016/j.ijporl.2019.04.019. Epub 2019 Apr 17.
10
Acute flaccid paraparesis (cauda equina syndrome) in a patient with Bardet-Biedl syndrome.
Indian J Orthop. 2017 May-Jun;51(3):330-333. doi: 10.4103/0019-5413.205682.

引用本文的文献

2
NGS and phenotypic ontology-based approaches increase the diagnostic yield in syndromic retinal diseases.
Hum Genet. 2021 Dec;140(12):1665-1678. doi: 10.1007/s00439-021-02343-7. Epub 2021 Aug 26.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验