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Table 1 Pheno- and genotype distribution among HHT patients

From: 20-year follow-up study of Danish HHT patients—survival and causes of death

 

All HHT patients

Male

Female

Number

73

34

39

Age 1 January 1995 (range)

53.8 (14–88)

51.5 (18–88)

55.5 (14–87)

PAVM diagnosed at CT or Pulmonary angiography

23

9

14

HHT1

38

18

20

HHT2

24

14

10

JP-HHT

0

0

0

Unknown type

11

2

9

Died in the follow-up period

32

13

19

HHT stated as cause of death

6

3

3

Cancer stated as cause of death

3

1

2

Other HHT related diagnosis stated as cause of death

10

6

4

  1. Abbreviations: PAVM Pulmonary arteriovenous malformations, HHT1 Hereditary Hemorrhagic Telangiectasia type 1, HHT2 Hereditary Hemorrhagic Telangiectasia type 2, HHT- JP Hereditary Hemorrhagic Telangiectasia and Juvenile Polyposis