SR302

SECORD (IA2b)

Female

Female

SR302

SECORD (IA2b)

Female

Female

Highlighted Images

Age at visit: 6 years
OD OS

History

This 6 year old girl has had poor acuity her entire life. At a few months of age, her parents noticed her nystagmus and sought medical attention.

Refraction OD:     +5.50 +1.25 x 102
Refraction OS:     +4.75 +1.25 x 072

Pedigree

Teaching Points

The clinical features supporting the diagnosis of severe early childhood onset retinal dystrophy (SECORD) in this patient include: nystagmus noted shortly after birth; reduced acuity for her entire life, a non-recordable ERG, legal blindness before age 10 (visual field criteria), a relatively normal fundus appearance with pink optic disks; hyperopia; and, normally sighted parents.

Age at visit: 6 years
Age at visit: 7 years
Age at visit: 9 years

Diagnosis & molecular findings

Disease Gene Allele 1 variant(s) Allele 2 variant(s) Inheritance mode
SECORD CEP290 IVS26+1655 A>G IVS26+1655 A>G AR
Disease:
Gene:
Allele 1:
IVS26+1655 A>G
Allele 2:
IVS26+1655 A>G
Inheritance:
AR
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