Phenotype #0000130127

Individual ID	00165248
Associated disease	MGR1
Phenotype details	The patient had 3 to 10 daily episodes of transient blindness, most commonly bilaterally, since infancy. He also had migraine with aura, the attacks would begin with a scintillating scotoma, followed by unilateral sensory symptoms and weakness, initially in one limb,progressing to include the trunk, the second limb and the face. Aphasia may have occurred. The attacks lasted ca.30 minutes and were followed by 1 to 8 hours of intense pulsatile headache, photophobia and phonophobia, nausea and occasional vomiting.
Diagnosis/Initial	FHM
Inheritance	-
Diagnosis/Definite	FHM-3
Age/Examination	-
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	Paola Carrera
Database submission license	No license selected
Created by	Paola Carrera
Date created	2012-07-25 13:05:18 +02:00 (CEST)
Date last edited	2018-07-06 17:14:08 +02:00 (CEST)

Global Variome shared LOVD