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A novel disorder involving dyshematopoiesis, inflammation, and HLH due to aberrant CDC42 function

Title: A novel disorder involving dyshematopoiesis, inflammation, and HLH due to aberrant CDC42 function
Authors: Lam M. T.; Coppola S.; Krumbach O. H. F.; Prencipe G.; Insalaco A.; Cifaldi C.; Brigida I.; Zara E.; Scala S.; Di Cesare S.; Martinelli S.; Di Rocco M.; Pascarella A.; Niceta M.; Pantaleoni F.; Ciolfi A.; Netter P.; Carisey A. F.; Diehl M.; Akbarzadeh M.; Conti F.; Merli P.; Pastore A.; Levi Mortera S.; Camerini S.; Farina L.; Buchholzer M.; Pannone L.; Cao T. N.; Coban-Akdemir Z. H.; Jhangiani S. N.; Muzny D. M.; Gibbs R. A.; Basso-Ricci L.; Chiriaco M.; Dvorsky R.; Putignani L.; Carsetti R.; Janning P.; Stray-Pedersen A.; Erichsen H. C.; Horne A.; Bryceson Y. T.; Torralba-Raga L.; Ramme K.; Rosti V.; Bracaglia C.; Messia V.; Palma P.; Finocchi A.; Locatelli F.; Chinn I. K.; Lupski J. R.; Mace E. M.; Cancrini C.; Aiuti A.; Ahmadian M. R.; Orange J. S.; De Benedetti F.; Tartaglia M.
Contributors: Lam, M. T.; Coppola, S.; Krumbach, O. H. F.; Prencipe, G.; Insalaco, A.; Cifaldi, C.; Brigida, I.; Zara, E.; Scala, S.; Di Cesare, S.; Martinelli, S.; Di Rocco, M.; Pascarella, A.; Niceta, M.; Pantaleoni, F.; Ciolfi, A.; Netter, P.; Carisey, A. F.; Diehl, M.; Akbarzadeh, M.; Conti, F.; Merli, P.; Pastore, A.; Levi Mortera, S.; Camerini, S.; Farina, L.; Buchholzer, M.; Pannone, L.; Cao, T. N.; Coban-Akdemir, Z. H.; Jhangiani, S. N.; Muzny, D. M.; Gibbs, R. A.; Basso-Ricci, L.; Chiriaco, M.; Dvorsky, R.; Putignani, L.; Carsetti, R.; Janning, P.; Stray-Pedersen, A.; Erichsen, H. C.; Horne, A.; Bryceson, Y. T.; Torralba-Raga, L.; Ramme, K.; Rosti, V.; Bracaglia, C.; Messia, V.; Palma, P.; Finocchi, A.; Locatelli, F.; Chinn, I. K.; Lupski, J. R.; Mace, E. M.; Cancrini, C.; Aiuti, A.; Ahmadian, M. R.; Orange, J. S.; De Benedetti, F.; Tartaglia, M.
Publisher Information: NLM (Medline); New York; USA
Publication Year: 2019
Collection: Sapienza Università di Roma: CINECA IRIS
Subject Terms: CDC42; dyshematopoiesi; inflammation; RHO-GTPase
Description: Hemophagocytic lymphohistiocytosis (HLH) is characterized by immune dysregulation due to inadequate restraint of overactivated immune cells and is associated with a variable clinical spectrum having overlap with more common pathophysiologies. HLH is difficult to diagnose and can be part of inflammatory syndromes. Here, we identify a novel hematological/autoinflammatory condition (NOCARH syndrome) in four unrelated patients with superimposable features, including neonatal-onset cytopenia with dyshematopoiesis, autoinflammation, rash, and HLH. Patients shared the same de novo CDC42 mutation (Chr1:22417990C>T, p.R186C) and altered hematopoietic compartment, immune dysregulation, and inflammation. CDC42 mutations had been associated with syndromic neurodevelopmental disorders. In vitro and in vivo assays documented unique effects of p.R186C on CDC42 localization and function, correlating with the distinctiveness of the trait. Emapalumab was critical to the survival of one patient, who underwent successful bone marrow transplantation. Early recognition of the disorder and establishment of treatment followed by bone marrow transplant are important to survival.
Document Type: article in journal/newspaper
Language: English
Relation: info:eu-repo/semantics/altIdentifier/pmid/31601675; info:eu-repo/semantics/altIdentifier/wos/WOS:000523636900008; volume:216; issue:12; firstpage:2778; lastpage:2799; numberofpages:22; journal:THE JOURNAL OF EXPERIMENTAL MEDICINE; http://hdl.handle.net/11573/1338555
DOI: 10.1084/jem.20190147
Availability: http://hdl.handle.net/11573/1338555; https://doi.org/10.1084/jem.20190147
Rights: info:eu-repo/semantics/openAccess
Accession Number: edsbas.CDDA2190
Database: BASE