Episodic angioedema with eosinophilia (Gleich's syndrome) associated with urticarial vasculitis: a coincidence or a novel clinical entity?

Autor: Basso, J.R., Bizinoto, L.G.Z., Limone, G.A., Enokihara, M.M.S.S., Espirito-Santo Filho, K. do, Fonseca, A.R., Agondi, R.C., Gois, A.F.T. de, Cunha, L.L.

Publikováno v: Brazilian Journal of Medical and Biological Research v.54 n.6 2021
Brazilian Journal of Medical and Biological Research
Associação Brasileira de Divulgação Científica (ABDC)
instacron:ABDC
Brazilian Journal of Medical and Biological Research, Volume: 54, Issue: 6, Article number: e10745, Published: 19 APR 2021

Episodic angioedema with eosinophilia (EAE) is a rare condition characterized by recurrent attacks of angioedema and urticaria accompanied by a marked elevation of peripheral eosinophil count. We report the case of a young female patient diagnosed wi

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::170453c09e2537e286c8af8b0d7c00c9
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X2021000600501

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Evidence for the founder effect of RET533 as the common Greek and Brazilian ancestor spreading multiple endocrine neoplasia 2A

Autor: Cunha, L.L. Lindsey, S.C. França, M.I.C. Sarika, L. Papathoma, A. Kunii, I.S. Cerutti, J.M. Dias-Da-silva, M.R. Alevizaki, M. Maciel, R.M.B.

Objectives: About one-quarter of patients with medullary thyroid cancer (MTC) have inherited disease due to mutations in the RET gene. A rare mutation in exon 8 (G533C) of RET, previously described in a large Brazilian family with MEN2A, also appeare

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______2127::25e25bc3e319c76008c8aa7364f57de7
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3086526

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