Literature DB >> 21916343

Hereditary hemorrhagic telangiectasia: children need screening too.

Lynne A Sekarski1, Lori A Spangenberg.   

Abstract

Hereditary hemorrhagic telangiectasia (HHT) is an autosomal dominant blood vessel disorder characterized by the presence of arteriovenous malformations (AVMs), epistaxis, and mucocutaneous telangiectases. AVMs are present in lungs, brain, liver, and spine. Children and adults share the same manifestations, with epistaxis and skin telangiectases being the most common. Parents often seek medical attention for their children after an adult in the family is diagnosed. There is debate whether manifestations of HHT are present at birth or develop after puberty, thus making recommendations for evaluation or screening of children in families with HHT uncertain. In the authors' pediatric HHT center, potentially life-threatening manifestations of HHT have been identified in asymptomatic children under 12 years of age. Treatments for HHT include embolization and surgery, laser, and hormone therapy. It is imperative for nurses and other health professionals to recognize this disease and become familiar with evaluation and treatment options.

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Mesh:

Year:  2011        PMID: 21916343

Source DB:  PubMed          Journal:  Pediatr Nurs        ISSN: 0097-9805


  3 in total

1.  Recurrent erysipelas led to diagnosis of hereditary hemorrhagic telangiectasia.

Authors:  Mari Yamaoka; Yohei Kanzawa; Shun Tatehara; Koji Sasaki; Shimpei Mizuki; Jun Ohnishi; Takahiro Nakajima; Naoto Ishimaru; Saori Kinami
Journal:  Infez Med       Date:  2022-03-01

Review 2.  Standard anticoagulation for mesenteric vein thrombosis, revealing a 'zebra' diagnosis: hereditary haemorrhagic telangiectasia--the dripping truth!

Authors:  Aakash Aggarwal; Arundeep Singh Kahlon; Meghan Rane; Emerald Banas
Journal:  BMJ Case Rep       Date:  2013-10-28

3.  A long diagnostic delay in patients with Hereditary Haemorrhagic Telangiectasia: a questionnaire-based retrospective study.

Authors:  Paola Pierucci; Gennaro M Lenato; Patrizia Suppressa; Patrizia Lastella; Vincenzo Triggiani; Raffaella Valerio; Mario Comelli; Daniela Salvante; Alessandro Stella; Nicoletta Resta; Giancarlo Logroscino; Francesco Resta; Carlo Sabbà
Journal:  Orphanet J Rare Dis       Date:  2012-06-07       Impact factor: 4.123

  3 in total

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