The clinical profiles of individuals from a large Israeli-Arab family with the ENG mutation c.932T→G
| Patient | Age | Clinical profile |
|---|---|---|
| C, cerebral AVM; E, epistaxis; G, gastrointestinal bleeds; P, pulmonary AVM; T, telangiectases. | ||
| 1573 | 34 | E, T, P, C, amnesia, hemiplegia |
| 1576 | 5 | Developmental delay, asymptomatic for HHT manifestations |
| 1628 | 54 | E, T, P, C |
| 1629 | 6 | E |
| 1632 | 8 | E, T |
| 1633 | 32 | E, T, C, G, liver abscess |
| 1637 | 7 | E |
| 1642 | 56 | E, T |
| 1644 | 31 | E, T |
| 1648 | 33 | E, T, C |
| 2698 | 36 | E, T, P, brain abscess |
| 2700 | 1 | Asymptomatic |