Phenotype #0000305564

Individual ID 00413590
Associated disease -
Phenotype details best corrected visual acuity first visit (age), follow up visit: fixates and follows (2), 20/80; refraction at follow-up: -1.50 = 1.50x130, +1 = 1x85212; full-field electroretinography at presentation, at follow-up - right eye; rod amplitude (A): 34, 87rod implicit time (it): 138, 122; rod-cone a wave (A): 135, 238; rod-cone a wave (it): 22, 17; rod-cone b wave (A): 105, 195; rod-cone b wave (it): 62, 31; cone a wave (A): 70, 75; cone a wave (it): 22, 18; cone b wave (A): 70, 81; cone b wave (it): 44, 37; 30 Hz flicker (A): 17, 18; 30 Hz flicker (it): 36, 29; red b1 (A): 27, 36; red b1 (it): 63, 65; normal values (respectively, range) 215-245, 103-380, 69-115, 164-378, 11-17, 284-705, 42-60, 54-117, 11-15, 96-239, 33-37, 96-259, 25-32, 51-197 , 42-53
Diagnosis/Initial -
Inheritance Familial, autosomal dominant
Diagnosis/Definite cone-rod dystrophy
Age/Examination 9y (9 years)
Age/Diagnosis -
Age/Onset -
Phenotype/Onset poor night vision, defective color vision, light sensitivity
Protein -
Owner name LOVD
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Anna Tracewska
Date created 2022-07-19 20:59:03 +02:00 (CEST)
Date last edited N/A

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