| Literature DB >> 24333532 |
Kerstin Felgentreff1, Matthias Siepe2, Stefan Kotthoff3, Yskert von Kodolitsch4, Kristina Schachtrup5, Luigi D Notarangelo6, Jolan E Walter7, Stephan Ehl8.
Abstract
Loeys-Dietz syndrome (LDS) is a connective tissue disorder caused by monoallelic mutations in TGFBR1 and TGFBR2, which encode for subunits of the transforming growth factor beta (TGFβ) receptor. Affected patients are identified by vascular aneurysms with tortuosity and distinct morphological presentations similar to Marfan syndrome; however, an additional predisposition towards asthma and allergy has recently been found. We describe two patients with a novel missense mutation in TGFBR1 presenting with highly elevated levels of IgE and severe eczema similar to autosomal-dominant Hyper-IgE syndrome (HIES). Mild allergic manifestations with normal up to moderately increased IgE were observed in 3 out of 6 additional LDS patients. A comparison of this cohort with 4 HIES patients illustrates the significant overlap of both syndromes including eczema and elevated IgE as well as skeletal and connective tissue manifestations.Entities:
Keywords: Allergy; EBV; EDS; Eczema; Ehlers–Danlos syndrome; Epstein–Barr virus; HIES; Hyper-IgE; Hyper-IgE syndrome; LDS; Loeys–Dietz syndrome; MFS; Marfan syndrome; T(reg); TAAD; TGF-beta; TGFBR; TGFβ; Transforming growth factor beta receptor; regulatory T cells; thoracic aortic aneurysm and dissections; transforming growth factor beta
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Year: 2013 PMID: 24333532 DOI: 10.1016/j.clim.2013.11.008
Source DB: PubMed Journal: Clin Immunol ISSN: 1521-6616 Impact factor: 3.969