Phenotype #0000060864

Individual ID	00081292
Associated disease	SLS
Phenotype details	HP:0007503 (Generalized Ichthyosis, Extremities: severe, Trunk: severe Face: mild); HP:0002313 (Spastic paraparesis, moderate, moderate gait abnormality); HP:0005750 (Contractures of the joints of the lower limbs, mild) HP:0001249 (intellectual disability, mild); HP:0001260 (Dysarthria, mild); HP:0007663 (Reduced visual acuity, right: 6/12, left: 6/18); HP:0030507 (retinal crystals); HP:0000551 (Abnormality of color vision, mild); HP:0007266 (Cerebral dysmyelination, moderate, frontal, parietal and periventricular); H-MRS lipid peak at 1.3 ppm (Lipid/Creatine-Ratio: 1.3)
Diagnosis/Initial	-
Inheritance	Familial, autosomal recessive
Diagnosis/Definite	-
Age/Examination	16y (16 years)
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	Maximilian Weustenfeld
Database submission license	No license selected
Created by	Maximilian Weustenfeld
Date created	2016-09-29 13:49:55 +02:00 (CEST)
Date last edited	2017-10-16 21:42:50 +02:00 (CEST)

Global Variome shared LOVD