Table 1 Published associations in Peters anomaly
AUTHORS | YEAR | TITLE | CONCULSION |
|---|---|---|---|
Shanske AL et al. | 2002 | Possible new syndrome of microcephaly with cortical migration defects, Peters anomaly and multiple intestinal atresias: a multiple vascular disruption syndrome [10] | New multiple associations-nervous and gastrointestinal |
Banning CS et al. | 2005 | Corneal perforation with secondary congenital aphakia in Peters anomaly [11]. | Ocular association |
Neilan E et al. | 2006 | Peters anomaly in association with multiple midline anomalies and a familial chromosome 4 inversion [12] | New multiple associations- orofacial, cardiac, nervous |
Navneet T et al. | 2009 | Peters plus syndrome and absence of kidney: a case report [13] | New association- unilateral renal agenesis |
Aliferis K et al. | 2010 | A novel nonsense B3GALTL mutation confirms Peters plus syndrome in a patient with multiple malformations and Peters anomaly [14] | Confirmed specific mutation in peters plus syndrome |
Shimizu R et al. | 2010 | Severe Peters plus syndrome-like phenotype with anterior eye staphyloma and hypoplastic left heart syndrome: proposal of a new syndrome [15] | New multiple associations-ocular and cardiovascular |
Lim Z, Quah BL | 2010 | Unilateral retinoblastoma in an eye with Peters anomaly [16] | Ocular association and a specific gene mutation |
Arikawa A et al. | 2010 | Case of novel PITX2 gene mutation associated with Peters' anomaly and persistent hyperplastic primary vitreous [17] | Ocular association and a specific gene mutation |
Sawada M et al. | 2011 | A case of aniridia with unilateral Peters anomaly [18] | New association- aniridia Genetic link- PAX 6 mutation |