Table 2

Renal and ocular features of patients with IgA glomerulonephritis or Alport syndrome

(A) IgA glomerulonephritis
Patient	Sex	Age	Haem	Pro	BP	Renal function	Cornea	Lens	Retina
JJ	F	37	+	+	ABN	N	N	N	0 dots
LJ	F	64	+	+	N	N	dots	N	0 dots
JB	M	58	+	+	N	ABN	N	N	100 dots
JM	M	39	+	+	N	N	N	N	0 dots
FE	F	46	+	+	N	ABN	N	N	0 dots
FD	F	38	−	−	N	N	N	N	0 dots
CL	M	23	+	−	N	N	N	N	0 dots
HP	M	51	+	−	N	N	N	N	0 dots
TW	M	51	+	+	N	ABN	N	N	0 dots
GJ	M	44	+	+	ABN	ABN	N	N	1 dot
FR	F	No further details		N	N	0.5 dots

(B) X linked Alport syndrome
Patient	Sex	Age (years)	FH	Hearing	Renal function	Age at renal failure	Cornea	Lens	Retina
DH	M	17	+	Abn	N, haem	NA	Corneal dystrophy	Dots	1 dot
PH	F	45	+	N	N, haem	NA	Corneal dystrophy	N	0.5 dot
JT	F	46	+	N	N, haem	NA	N	Opacity	6 dots
NH	M	30	−	Abn	Transplant	15	Dots	Scissor’s reflex	Dots and flecks
AC	M	34	−	Abn	Transplant	17	N	N	Dots and flecks
CH	F	37	+	N	N, haem	NA	N	N	1 dot

Haem = + RBC greater than × 10⁶/l; Pro = proteinuria + more than 0.3 g/day; BP + = blood pressure more than 140/90 mm Hg; FH = family history; N = normal; Abn = abnormal; NA = not applicable.
↵PH and DH are mother and son; electron microscopy of PH’s renal biopsy was typical of Alport syndrome, but DH has not had a biopsy.