SR84

ECORD (IA2c)

Male

Male

SR84

ECORD (IA2c)

Male

Male

Highlighted Images

Age at visit: 7 years
OD OS

History

This 5 year old boy has constricted visual fields that were first noticed when he started to walk (before age 1 year).

Refraction OD:     +3.50 +1.75 x 140
Refraction OS:     +3.00 +2.00 x 50

Pedigree

Teaching Points

The clinical features supporting the diagnosis of early childhood onset retinal dystrophy (ECORD) in this patient include: constricted visual fields noticed in the first year of life; reduced acuity, a non-recordable ERG, pink optic nerve heads; hyperopia; and, normally sighted parents.

Age at visit: 5 years
Age at visit: 7 years
Age at visit: 9 years
Age at visit: 9 years (Visit 2)
Age at visit: 11 years
Age at visit: 12 years
Age at visit: 13 years
Age at visit: 15 years
Age at visit: 17 years

Diagnosis & molecular findings

Disease Gene Allele 1 variant(s) Allele 2 variant(s) Inheritance mode
ECORD IQCB1 Glu346Stop GAG>TAG Arg72Stop CGA>TGA AR
Disease:
Gene:
Allele 1:
Glu346Stop GAG>TAG
Allele 2:
Arg72Stop CGA>TGA
Inheritance:
AR
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