PT  - JOURNAL ARTICLE
AU  - M E Porteous
AU  - J Burn
AU  - S J Proctor
TI  - Hereditary haemorrhagic telangiectasia: a clinical analysis.
AID  - 10.1136/jmg.29.8.527
DP  - 1992 Aug 01
TA  - Journal of Medical Genetics
PG  - 527--530
VI  - 29
IP  - 8
4099  - http://jmg.bmj.com/content/29/8/527.short
4100  - http://jmg.bmj.com/content/29/8/527.full
SO  - J Med Genet1992 Aug 01; 29
AB  - Data from 98 patients with hereditary haemorrhagic telangiectasia (HHT) are presented. All were symptomatic by 40 years of age and 62% by 16 years. Nose bleeding was the first symptom of disease in 90% of cases with mucocutaneous telangiectases appearing 5 to 20 years later. Complications of HHT are discussed and an age of onset curve given.