Table 1.

Clinical features

Case	Sex	Age at presentation	Clinical features	B/L or U/L	Systemic features	Clinical diagnosis
1 (KL)	F	3 days	Diffuse panstromal corneal clouding (see Fig 1)	B/L	Nil	Congenital glaucoma
2 (CC)	M	5 days	RE complete opaque cornea (see Fig 5)	U/L	CHARGE syndrome	Sclerocornea
					Bilateral choanal atresia ASD, VSD, coarctation of aorta, micropenis
3 (CC)		20 days	RE opaque enlarged cornea with stromal vascularisation	U/L	Nil	Peters' anomaly
			? Keratolenticular adhesion
4 (KP)	F	4 days	B/L dense central corneal opacities with peripheral irido-corneal adhesions	B/L	Orofacial digital syndrome	Peters' anomaly
					Cleft lip and palate, brachycephaly, short femurs, brachydactyly, clinodactyly
5 (MG)	M	4 days	B/L corneal opacification with a central area of relative ectasia posterior embryotoxon (see Fig 3)	B/L	Nil	Corneal ectasia
6 (SH)	F	7 days	LE central corneal opacity with irido-corneal touch	U/L	Nil	Peters' anomaly
7 (VCN)	M	7 days	B/L scleralised corneas temporally	B/L	Nil	Sclerocornea
8 (EF)	M	5 days	Opaque corneas HCD 11 mm R and 11.5 mm L	B/L	Nil	Congenital glaucoma
9 (NS)	M	7.5 months	B/L opaque corneas with evidence of scleralisation	B/L	Nil	Sclerocornea
10 (ET)	M	6 weeks	B/L diffuse opaque corneas with complete scleralisation RE and some sparing inferiorly LE	B/L	Nil	Sclerocornea
11 (TH)	M	5 months	B/L diffuse opaque corneas with microcornea and scleralisation	B/L	Intrauterine growth retardation, failure to thrive	Sclerocornea
12 (RM)	M	7 days	B/L corneal ring opacities with thinning centrally	B/L	Peters' plus syndrome	Peters' anomaly
					B/L cleft lip and palate, rhizomelia, clinodactyly, long philtrum
13 (MR)	F	7 days	RE central corneal opacity	U/L	Nil	Peters' anomaly
			LE Axenfeld anomaly but clear cornea (see Fig 4)

HCD = horizontal corneal diameter, RE = right eye, LE = left eye, ASD = atrial septal defect, VSD = ventricular septal defect, U/L = unilateral, B/L = bilateral.