Results 41 to 50 of about 7,492,668 (163)

Seroprevalence of Toxoplasma gondii, Rubella Virus, Cytomegalovirus, and Herpes Simplex Virus Among Children and Women in Bhutan's National Referral Hospital: A Cross‐Sectional Study

Public Health Challenges, Volume 5, Issue 3, September 2026.
Congenital infections caused by Toxoplasma gondii, rubella virus, cytomegalovirus, and herpes simplex virus were assessed in 624 children and women at JDWNRH (2019–2022). HSV (83.8%) and CMV (82.7%) were most prevalent, whereas T. gondii was the lowest (14.7%).
Karma Norbu, Sonam Wangzin Rabjay, Karma Galey, Thinley Dorji, Ugyen Chophel, Jamyang Wangmo, Binita Rai, Yeshey Dorjey, Tshokey Tshokey   +8 more
wiley   +1 more source

Parvovirus B19 Prevalence among Children of African Descent in Sokoto North Western Nigeria

Sokoto Journal of Medical Laboratory Science, 2019
Human Parvovirus B19 (HPVB19) belongs to the family Parvoviridae and it causes Erythema infectiosum, aplastic crises in persons with blood disorder and prolonged anaemia in immuno compromised persons.
Ibrahim, K.* , Muhammad, M.B. , Erhabor, O. , Adias, T.C. , Udomah, F. , Abdulrahaman, Y. , Onuigwe, U. , Okwesili, A. , Ibrahim, B.A. , Buhari, H. , Zama, I. , Erhabor, T . Egenti, B.N.
doaj  

Primary infection by human parvovirus B19

, 1993
We describe a case of primary infection by human parvovirus B19 in a 20-year-old woman; it manifested as erythemato-maculo-papular lesions, pharyngotonsillitis, lymphadenopathy, fever, arthralgia and myalgia, asthenia and anorexia.
G. Lunghi, R. Cardone, S. Veraldi, G. Rizzitelli   +3 more
core   +1 more source

Phenotype‐specific immune profiles and outcomes in childhood autoimmune neutropenia: A 20‐year cohort study

British Journal of Haematology, Volume 209, Issue 3, Page 1158-1165, September 2026.
Summary Childhood autoimmune neutropenia (AIN) encompasses heterogeneous entities; phenotype‐specific immunological profiles and their relationship to infection outcomes remain incompletely defined. To characterise clinical, immunological and long‐term outcomes across distinct phenotypes of childhood AIN.
Ioanna Saougou, Chrysoula Kosmeri, Nikolaos Chaliasos, Irene Mavroudi, Charalampos Pontikoglou, Alexandros Makis   +5 more
wiley   +1 more source

H Syndrome Associated With Pure Red Cell Aplasia, Rosai–Dorfman Disease, and Sensorineural Hearing Loss: Phenotypic Variability in Three Children With the Same SLC29A3 Mutation

Clinical Case Reports, Volume 14, Issue 8, August 2026.
ABSTRACT H syndrome is a rare autosomal recessive disorder caused by mutations in the SLC29A3 gene. We report three pediatric patients with a homozygous c.1309G>A (p.Gly437Arg) mutation presenting with distinct phenotypic variations. These cases expand the clinical spectrum and emphasize the importance of early genetic diagnosis and family counseling.
Mohammad Najajrah, Hadeel I. Bouzia, Nermin K. Darawi, Fatima S. Hajjaj, Nour H. Moosa, Noor M. Awad   +5 more
wiley   +1 more source

PARVOVIRUS B19 IN HUMAN DISEASE

, 1997
▪ Abstract  Parvovirus B19, the only known human pathogenic parvovirus, is associated with a wide range of disease manifestations. In healthy individuals, the major presentation of B19 infection is erythema infectiosum.
K.E. Brown, MD, N.S. Young, MD
core   +1 more source

Preservative Monitoring of a Greek Woman with Hydrops Fetalis due to Parvovirus B19 Infection

Case Reports in Obstetrics and Gynecology, 2017
Primate erythroparvovirus 1 (parvovirus B19) is a member of the Erythrovirus genus of the Parvoviridae family and it is one of the few members of the family known to be pathogenic in human.
Zacharias Fasoulakis, Panagiotis Antsaklis, Emmanuel N. Kontomanolis   +2 more
doaj   +1 more source

Parvovirus B19 associated autoantibodies upregulation in women and children in Southern China

Journal of Laboratory Medicine, 2021
Human parvovirus B19, the cause of fifth disease in children and transient arthropathy in adults, could induce autoimmunity and the production of autoantibodies.
Yu Qing, Tan Ruhong, Zhao Jiayi, Zhou Qixian, Zheng Fen, Li Xiangxin   +5 more
doaj   +1 more source

Pediatric Pityriasis Lichenoides Chronica, A Rare Case Report

Clinical Case Reports, Volume 14, Issue 8, August 2026.
ABSTRACT Pityriasis lichenoides chronica (PLC) is a rare, chronic inflammatory skin disorder presenting as recurrent pruritic papulosquamous lesions. Accurate diagnosis requires clinical evaluation and histopathology. A multimodal treatment approach, including topical steroids, tacrolimus, narrowband UVB, and methotrexate, can achieve complete ...
Halkawt Babarasul Ahmed, Jeza Muhamad Abdul Aziz, Mohammed Kaka Bra Salih, Goran Mohammed Raouf, Parshal Bhandari   +4 more
wiley   +1 more source

FETO-PLACENTARY PATHOLOGY IN HUMAN PARVOVIRUS B19 INFECTION

, 1998
In view of the scarce references concerning the histological data in congenital parvovirus human B19 infection, we intend to provide a description of the pathological features observed in six autopsies.The virus was detected by DNA hybridization (ISH-DBH)
Maria Evangelina Ferreira FONSECA, Jussara Pereira NASCIMENTO, PEGADO, Claudia Schwartz, FONSECA, Maria Evangelina Ferreira, Cubel, Rita de Cassia, Claudia Schwartz PEGADO, NASCIMENTO, Jussara Pereira, Rita de Cassia Nasser CUBEL, SLOBODA, Ivan, Aparecida Gomes Pinto GARCIA, Ivan SLOBODA, GARCIA, Aparecida Gomes Pinto, CUBEL, Rita de Cassia Nasser   +12 more
core   +1 more source