Syndromic and Nonsyndromic Systemic Associations of Congenital Lacrimal Drainage Anomalies: A Major Review

被引:40
作者
Ali, Mohammad Javed [1 ,2 ]
Paulsen, Friedrich [2 ]
机构
[1] LV Prasad Eye Inst, Govindram Seksaria Inst Dacryol, Rd 2,Banjara Hills, Hyderabad 500034, Andhra Pradesh, India
[2] Friedrich Alexander Univ Erlangen Nurnberg, Inst Anat, Erlangen, Germany
关键词
NASOLACRIMAL DUCT OBSTRUCTION; RUBINSTEIN-TAYBI-SYNDROME; OBLIQUE FACIAL CLEFTS; LIMB MAMMARY SYNDROME; ECTODERMAL DYSPLASIA; OPHTHALMIC MANIFESTATIONS; OCULAR FINDINGS; SALIVARY-GLANDS; DOWN-SYNDROME; EEC-SYNDROME;
D O I
10.1097/IOP.0000000000000923
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Purpose: To review and summarize the syndromic, nonsyndromic, and systemic associations of congenital lacrimal drainage anomalies. Methods: The authors performed a PubMed search of all articles published in English on congenital lacrimal anomalies (1933-2016). Patients of these articles were reviewed along with the literature of direct references to syndromes and other systemic associations. Data reviewed included syndromic descriptions, systemic details, demographics, lacrimal presentations, management, and outcomes. Results: Syndromic and systemic associations with congenital lacrimal drainage disorders are not known to be common. Although familial presentations have been reported, the inheritance patterns are unclear for most anomalies. There is an increasingly growing evidence of a genetic basis to many lacrimal anomalies. However, few syndromes have either widespread or are frequently associated with lacrimal anomalies. Few sequences of distinct lacrimal presentations and intraoperative findings are seen. Surgical challenges in these patients are distinct and a thorough pre and intraoperative anatomical assessment, detailed imaging when indicated, and assessment and correction of associated periocular and facial abnormalities may facilitate good outcomes. Conclusions: Lacrimal drainage anomalies associated with syndromic and nonsyndromic systemic conditions have certain unique features of their own and their surgical and anesthesia challenges are distinct. Diagnosis of congenital lacrimal drainage anomalies should prompt consideration of the possible presence of associated systemic abnormalities.
引用
收藏
页码:399 / 407
页数:9
相关论文
共 173 条
[1]   Distinct Ocular Expression in Infants and Children With Down Syndrome in Cairo, Egypt Myopia and Heart Disease [J].
Afifi, Hanan H. ;
Azeem, Amira A. Abdel ;
El-Bassyouni, Hala T. ;
Gheith, Moataz E. ;
Rizk, Akmal ;
Bateman, J. Bronwyn .
JAMA OPHTHALMOLOGY, 2013, 131 (08) :1057-1066
[2]  
Aguirre Vila-Coro A, 1988, Arch Ophthalmol, V106, P454
[3]  
AKDEMIR H, 1991, ACTA OPHTHALMOL, V69, P680
[4]   Management of Unilateral Versus Bilateral Lacrimal Drainage System Dysfunction in Down Syndrome [J].
Al-Faky, Yasser H. ;
Mousa, Ahmad ;
Alkhiary, Hattan T. ;
Al-Mosallam, Abdul Rahman .
JOURNAL OF PEDIATRIC OPHTHALMOLOGY & STRABISMUS, 2012, 49 (02) :109-113
[5]   Management of congenital lacrimal (anlage) fistula [J].
Al-Salem, Khalil ;
Gibson, Andrew ;
Dolman, Peter J. .
BRITISH JOURNAL OF OPHTHALMOLOGY, 2014, 98 (10) :1435-1436
[6]  
Ali MJ., 2015, Principles and Practice of Lacrimal Surgery, V2nd, P9
[7]  
Ali MJ, 2017, ORBIT, V36, P137, DOI 10.1080/01676830.2017.1280059
[8]   Bilateral Lacrimal Mucoceles in a Setting of Congenital Arhinia [J].
Ali, Mohammad Javed .
OPHTHALMIC PLASTIC AND RECONSTRUCTIVE SURGERY, 2014, 30 (06) :E167-E167
[9]   Balloon dacryoplasty: ushering the new and routine era in minimally invasive lacrimal surgeries [J].
Ali, Mohammad Javed ;
Naik, Milind N. ;
Honavar, Santosh G. .
INTERNATIONAL OPHTHALMOLOGY, 2013, 33 (02) :203-210
[10]   A second family with blepharo-naso-facial syndrome [J].
Allanson, JE .
CLINICAL DYSMORPHOLOGY, 2002, 11 (03) :191-194