Phenotype #0000038919
Individual ID |
00052342 |
Associated disease |
CADASIL |
Phenotype details |
see paper; ..., migraine with aura, bipolar disorder, sarcoidosis, no history of (transient) neurological deficits, neurological examination normal, MMSE 28/30; brain MRI (axial T1, T2, proton density and sagittal FLAIR weighted images) showed partly confluent WMH in a pattern consistent with CADASIL, incl. anterior temporal lobes |
Diagnosis/Initial |
- |
Inheritance |
Familial, autosomal dominant |
Diagnosis/Definite |
- |
Age/Examination |
40y (40 years) |
Age/Diagnosis |
- |
Age/Onset |
- |
Phenotype/Onset |
- |
Protein |
- |
Owner name |
Martine van Belzen |
Database submission license |
No license selected |
Created by |
Elles Boon |
Date created |
2013-04-15 16:22:29 +02:00 (CEST) |
Date last edited |
2016-11-29 22:57:42 +01:00 (CET) |
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