Hereditary angioedema in children: A review and update

Neha Pancholy, Timothy Craig

Research output: Contribution to journalReview articlepeer-review

1 Scopus citations

Abstract

Purpose of review Hereditary angioedema (HAE) most often presents in the first two decades of life. Despite these patients often see multiple doctors and go many years before confirmation of the diagnosis. the impact on quality of life, productivity and risk of anxiety, depression, and posttraumatic stress emphasizes the need for early diagnosis and appropriate treatment. Recent findings Over the past decade, therapy in the USA has emerged from fresh-frozen plasma and androgens to more than seven medications that are specific for bradykinin-induced disease. During the same time, treatment has evolved from intravenous to subcutaneous and the future will be a focus on oral therapy.SummaryMuch optimism exists that patients with HAE will live a life with minimal disease and impact on their quality of life making it even more important to diagnose children at an early age.

Original languageEnglish (US)
Pages (from-to)863-868
Number of pages6
JournalCurrent opinion in pediatrics
Volume31
Issue number6
DOIs
StatePublished - Dec 1 2019

All Science Journal Classification (ASJC) codes

  • Pediatrics, Perinatology, and Child Health

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