Results 71 to 80 of about 5,957 (204)

Additional file 2 of Germline 3p22.1 microdeletion encompassing RPSA gene is an ultra-rare cause of isolated asplenia

, 2021
Additional file 2: Fig. S1. Additional evidence for causative role of the de novo deletion 3p22.1. A—NGS results using IGV software showing homozygosity for all genetic variations found at locus. RPSA in patient with asplenia.
Sylwia Kołtan (8955506), Katarzyna Bąbol-Pokora (11710986), Aleksandra Oszer (11710983), Wojciech Młynarski (11710989), Agata Pastorczak (9133733)   +4 more
core   +1 more source

A Rare Association of Congenital Asplenia with Jejunal Arteriovenous Malformation

, 2017
BACKGROUND Isolated congenital asplenia is a poorly understood and rare form of primary immunodeficiency, often associated with life-threatening infections. CASE REPORT We encountered a unique case of a 22-year-old asplenic male who presented with severe
Mazhar, Areej, Arnautovic, Jelena Z, Tereziu, Stela, Gupta, Kashvi   +3 more
core  

Left atrial isomerism associated with asplenia: Prenatal echocardiography detection of complex congenital cardiac malformations

, 1984
Complex congenital heart disease with suspected isomerism of the atria was diagnosed in two fetuses of 20 and 29 weeks' gestation using two-dimensional and M-mode scanning techniques.
Juriy W. Wladimiroff, Wladimiroff, J. W., Stewart, Patricia A., Patricia A. Stewart, Becker, Anton E., Essed, C. E., Essed, Catharina E., Stewart, P. A., Wladimiroff, Juriy W., Becker, A. E., Anton E. Becker, Catharina E. Essed   +11 more
core   +1 more source

Severe Nasofacial Necrosis From Capnocytophaga canimorsus: A Case Report of Disease and Reconstruction

Eye &ENT Research, Volume 3, Issue 1, Page 33-36, March 2026.
Armon Hadian, Jason Azzi, Benjamin Taylor   +2 more
wiley   +1 more source

Campylobacter jejuni bacteremia in a patient with asplenia and enteritis

IDCases, 2019
Campylobacter bacteremia is an unusual presentation of a common infectious disease such as enteritis. We provide key teaching points about its presentation, risk factors, diagnosis and treatment.
Ramírez Isabel
doaj   +1 more source

A rare case of heme oxygenase deficiency: A case report and literature review

Clinical Case Reports
Key Clinical Message Heme oxygenase deficiency, a rare condition disrupting heme metabolism, has only nine reported cases. We present a 3‐year‐old boy with dysmorphic facies, asplenia, and normal bilirubin levels despite ongoing hemolysis.
Sai Santhosha Mrudula Alla, Pahel Agarwal, Dhruv J. Shah, Waseem Abrar Shajahan, Rakshna Ramsundar, Deekshitha Alla, Madhavi Ravulapalli, Satya Bora, Sanjay Pillai, Ruth G. Bayeh, Uday Kumar Repalle, Fnu Suhani   +11 more
doaj   +1 more source

Severe Legionnaires’ Disease Complicated by Rhabdomyolysis and Clinically Resistant to Moxifloxacin in a Splenectomised Patient: Too Much of a Coincidence?

Case Reports in Infectious Diseases, 2015
We here report a case of Legionnaires’ disease in a splenectomised patient, complicated by rhabdomyolysis and acute renal failure and characterized by a poor clinical response to moxifloxacin.
Theocharis Koufakis, Ioannis Gabranis, Marianneta Chatzopoulou, Anastasios Margaritis, Maria Tsiakalou   +4 more
doaj   +1 more source

Field Observation Of Egg Brooding In The Caecilian Caudacaecilia Asplenia From Sabah, Malaysia (Amphibia: Gymnophiona: Ichthyophiidae)

, 2008
Nishikawa, Kanto, Matsui, Masafumi, Imbun, Paul Y., Sudin, Ahmad (2008): Field Observation Of Egg Brooding In The Caecilian Caudacaecilia Asplenia From Sabah, Malaysia (Amphibia: Gymnophiona: Ichthyophiidae).
Imbun, Paul Y., Nishikawa, Kanto, Matsui, Masafumi, Sudin, Ahmad   +3 more
core   +1 more source

Szczepienia ochronne u dorosłych chorych na nowotwory hematologiczne, u chorych z asplenią oraz chorych na nocną napadową hemoglobinurię– zalecenia PTHiT i sekcji do spraw zakażeń PALG

Acta Haematologica Polonica
Infections are among the most common causes of morbidity and mortality in patients with hematological malignancies, and proper immunization can significantly reduce their incidence.
Iwona Hus, Agnieszka Piekarska, Katarzyna Brzeźniakiewicz-Janus, Krzysztof Giannopoulos, Krzysztof Jamroziak, Patrycja Mensah-Glanowska, Beata Piątkowska-Jakubas, Jacek Roliński, Krzysztof Tomasiewicz, Agnieszka Wierzbowska, Jan Maciej Zaucha, Sebastian Giebel, Lidia Gil   +12 more
doaj   +1 more source

Pneumococcal infection transmission between family members with congenital asplenia: A case report [PDF]

, 2019
BACKGROUND Asplenia, the lack of a spleen, can be congenital and increases susceptibility to severe infections caused by encapsulated bacteria, such as Streptococcus pneumoniae (S. pneumoniae).
Hiramatsu, Kazuhiro, Kato, Takehito, Shibata, Jumpei, Kenzaka, Tsuneaki   +3 more
core   +1 more source