AI Article Synopsis

  • Hereditary haemorrhagic telangiectasia (HHT) is an inherited disorder caused by mutations in specific genes (ACVRL1, ENG, SMAD4) and is characterized by abnormal blood vessel formations.
  • Patients typically display small arteriovenous malformations (AVMs) on the skin and in the gastrointestinal tract, along with larger AVMs in vital organs like the lungs and brain, but symptoms can vary widely.
  • The report highlights two unique cases of patients with no family history of HHT, who are mosaic for gene mutations and emphasize the importance of recognizing genetic mosaicism in diagnosing and testing for HHT.

Article Abstract

Hereditary haemorrhagic telangiectasia (HHT) is an autosomal dominant disorder caused by mutations in the ACVRL1, ENG, and SMAD4 genes. HHT is commonly characterised by small arteriovenous malformations (AVMs) known as telangiectasias of the skin, oral or gastrointestinal mucosa, as well as larger AVMs of solid organs (lungs, liver, brain). However, the manifestations of HHT are extremely variable. Two patients with no family history of HHT and strikingly different clinical presentations, who are mosaic for mutations in the ACVRL1 or ENG gene, are reported here. These cases represent the first report of mosaicism in patients clinically affected with classical HHT and pulmonary arterial hypertension, and suggest the need for awareness of mosaicism when performing clinical testing for this disorder.

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Source
http://dx.doi.org/10.1136/jmg.2010.088286DOI Listing

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