Results 91 to 100 of about 54,540 (236)

European S2k guidelines on management of autoimmune blistering diseases in children and adolescents

Journal of the European Academy of Dermatology and Venereology, Volume 40, Issue 7, Page 1137-1161, July 2026.
Autoimmune blistering disorders (AIBDs) in children are rare, challenging to diagnose and treat and often require immunosuppressants. Until now, no paediatric care guidelines existed. The EADV Task Force for AIBDs has developed the consensus‐based recommendations, enabling physicians to adopt a uniform, tailored treatment strategy to improve outcomes ...
A. Nanda, B. Tedbirt, C. Bodemer, M. C. Bolling, M. El Hachem, M. Nikolić, E. Benton, M. Caproni, D. De, D. Didona, K. Drenovska, M. Goebeler, M. Hertl, B. Horváth, M. Kasperkiewicz, D. Kiritsi, M. Larralde, A. V. Marzano, J. Meijer, D. F. Murrell, J. Powell, E. Sprecher, N. S. Chandran, M. M. Tomayko, S. Uzun, N. van Beek, H. Ott, A. Patsatsi, A. Torrelo, A. Welfringer‐Morin, E. Schmidt, P. Joly   +31 more
wiley   +1 more source

Effect of Home‐Based Multiple Micronutrient Powder Fortification on Haemoglobin Levels in Infants in Nampula, Mozambique: A Pragmatic Clinical Trial

Maternal &Child Nutrition, Volume 22, Issue 3, July 2026.
ABSTRACT To conduct a pragmatic clinical trial with multiple micronutrient powders (MNPs) for anaemia prevention during the first year of life in primary care in Nampula, Mozambique. A total of 275 infants, aged 6–8 months, were randomly assigned to intervention (IG, n = 145) and control (CG, n = 130) groups. The IG received 90 sachets of MNP for daily
Ana Raquel Ernesto Manuel Gotine, Marly Augusto Cardoso   +1 more
wiley   +1 more source

Insights Into the Susceptibility of Fungal Infection and STAT3 Genetic Mutations

Mycoses, Volume 69, Issue 7, July 2026.
ABSTRACT Signal transducer and activator of transcription 3 (STAT3) is a key transcription factor that regulates a spectrum of genes and signalling pathways critical for the antifungal immune response. Mutations in the STAT3 gene confer susceptibility to severe and recurrent fungal infections, predominantly via disruption of interleukin‐17 (IL‐17 ...
Fengming Li, Xiaodong Liu, Yuanyuan Li, Jie Wu, Ningning Dang, Jing Guo   +5 more
wiley   +1 more source

Expanding the PKLR mutation spectrum: discovery of two novel variants in two pediatric cases of pyruvate kinase deficiency

Annals of Hematology
Diagnosing neonatal pyruvate kinase (PK) deficiency is challenging, especially when early transfusions render conventional testing inconclusive. Genetic testing, however, is not influenced by transfusions and can provide, in most cases, a definitive ...
Oliver Sakalian, Yoann Huguenin, Serge Pissard, Vanessa Augis, Laurent Weinmann, Valérie Fuster, Marie Lagarde, Elise Badour, Nathalie Aladjidi, Julian Boutin, Stéphanie Dulucq   +10 more
doaj   +1 more source

Case of Autoimmune Haemolytic Anaemia in a One Month Old Child with Congenital Cytomegalovirus Infection (cCMV) [PDF]

Liaquat National Journal of Primary Care
Here we report a case of congenital CMV infection with rare presentation as haemolytic anaemia in a 50-day-old infant. Clinical manifestations of our patient were pallor, jaundice, hepatosplenomegaly, and a deranged coagulation profile.
Tahniat Shakil, Saima Gillani, Sohail Khan, Saad Hussain   +3 more
doaj   +1 more source

Clinical Outcomes of Splenectomy in Children: Report of the Splenectomy in Congenital Hemolytic Anemia (SICHA) Registry

American journal of hematology/oncology, 2014
The outcomes of children with congenital hemolytic anemia (CHA) undergoing total splenectomy (TS) or partial splenectomy (PS) remain unclear. In this study, we collected data from 100 children with CHA who underwent TS or PS from 2005 to 2013 at 16 sites
H. Rice, B. Englum, J. Rothman, S. Leonard, A. Reiter, C. Thornburg, M. Brindle, N. Wright, M. Heeney, C. Smithers, Rebeccah L. Brown, T. Kalfa, J. Langer, M. Cada, K. Oldham, J. Scott, S. S. St. Peter, Mukta Sharma, A. Davidoff, K. Nottage, K. Bernabe, D. Wilson, S. Dutta, B. Glader, S. Crary, M. Dassinger, Levette N. Dunbar, S. Islam, Manjusha Kumar, F. Rescorla, S. Bruch, A. Campbell, M. Austin, R. Sidonio, M. Blakely   +34 more
semanticscholar   +1 more source

Adolescent with Alport syndrome and congenital hemolytic anemia

Nefrología (English Edition), 2023
Leonor García Maset, Sonia Santillán Garzón, Pedro Ortega López   +2 more
doaj   +1 more source

An Unusual Case of Multifactorial Hemolytic Anemia: A Complex Interaction Between Genetic and Autoimmune Factors

Hemato
Hemolytic anemias (HAs) encompasses a heterogeneous group of disorders with either congenital or acquired etiologies. We present a complex case of a 27-year-old woman with hemolytic anemia of multifactorial origin, involving both inherited RBC membrane ...
Mario Biglietto, Giusy Peluso, Cristina Luise, Diletta Tripi, Maria Francesca Conforti, Valeria Filipponi, Luisa Bizzoni, Stefania Trasarti   +7 more
doaj   +1 more source

SPLENECTOMY IN SPLENIC ANEMIA, HEMOLYTIC ICTERUS AND HANOT'S CIRRHOSIS

, 1916
The value of splenectomy in splenic anemia remains unquestioned, and since the first report by Banti in 1894 sufficient time has now elapsed to enable us to draw definite conclusions regarding not only the immediate success, but also the permanency, of ...
Joseph L. Miller
semanticscholar   +1 more source

Idiopathic pulmonary hemosiderosis associated with Kabuki syndrome

Immunological Medicine
Kabuki syndrome (KS) is a genetic disorder caused by gene mutations in either lysine-specific methyltransferase 2D (KMT2D) or lysine demethylase 6A (KDM6A).
Yoji Uejima, Kenji Yoshida, Hirofumi Ohashi   +2 more
doaj   +1 more source