Table 3.
Heritable disorders associated with intracranial aneurysms.
| Disorder | Inheritance | Special features |
|---|---|---|
| α-Glucosidase deficiency | AR | Aneurysms often fusiform |
| α1-Antitrypsin deficiency | AR | Heterozygotes may be affected |
| Alkaptonuria | AR | |
| Anderson-Fabry disease | XLR | Aneurysms often fusiform; Carriers may be affected |
| Autosomal polycystic kidney disease | AD | |
| Ehlers-Danlos syndrome type IV | AD | |
| Familial idiopathic non-arteriosclerotic cerebral calcification syndrome | ? | |
| Hereditary hemorrhagic telangiectasia | AD | |
| Marfan's syndrome | AD | |
| Neurofibromatosis type 1 | AD | |
| Noonan's syndrome | AD | |
| Pseudoxanthoma elasticum | AD, AR | |
| Tuberous sclerosis | AD | Aneurysms often fusiform |
| Wermer's syndrome (multiple endocrine neoplasia type 1) | AD | |
| 3M syndrome | ? |
AD, autosomal dominant; AR, autosomal recessive; XLR, X-linked recessive.