Results 51 to 60 of about 7,492,718 (206)

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

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

High Prevalence of Parvovirus B19 IgG Antibody among Hemophilia Patients in Center for Special Diseases, Shiraz, Iran [PDF]

Iranian Journal of Public Health, 2005
Human parvovirus B19, the causative agent of fifth disease in childhood, is non-enveloped DNA virus and resistant to many physicochemical agents. B19 is a potential risk to hemophiliac patients receiving blood products. To determine the prevalence of the
M Mahmoodian Shooshtari, M Nabi Foroghi, R Hamkar   +2 more
doaj  

Seroprevalence of parvovirus B19 among pregnant women in Tripoli, Libya

Journal of Infection in Developing Countries, 2009
Background: Human parvovirus B19 has been implicated as a primary etiologic agent of erythema infectiosum (fifth disease) and aplastic crisis in patients with chronic haemolytic anemias. Human parvovirus B19 is known to be associated with adverse effects
Elfatah Elnifro, A.K. Nisha, Musbah Almabsoot, Ali Daeki, Nuri Mujber, Jose Muscat   +5 more
doaj   +1 more source

Deep intronic ANK1 variants causing pseudo‐exon inclusion in hereditary spherocytosis: Whole‐genome sequencing and functional assessment

British Journal of Haematology, EarlyView.
Victor Marin, Alexandre Janin, Céline Renoux, Yoann Huguenin, AURAGEN consortium, Stéphanie Dulucq, Louis Lebreton, Philippe Joly, Julian Boutin   +8 more
wiley   +1 more source

Nanomaterial‐Based CRISPR/Cas‐Powered Electrochemical Sensing Integrated With Microfluidics for Rapid and Sensitive Diagnostics

Electrochemical Science Advances, Volume 6, Issue 4, August 2026.
ABSTRACT Rapid and sensitive detection of disease‐related biomarkers is critical for early diagnosis and appropriate treatment. However, conventional analytical methods are often time‐consuming and require complex procedures and skilled personnel.
Minju Ahn, Sang Baek Sim, Izzati Haizan, Jin‐Ha Choi, Jeong‐Woo Choi   +4 more
wiley   +1 more source

Adult Reye-like syndrome associated with serologic evidence of acute parvovirus B19 infection

Brazilian Journal of Infectious Diseases, 2011
Reye's syndrome is an infrequently diagnosed medical condition affecting mainly children. The etiology, epidemiology and natural history of Reye's syndrome have been cloudily written in footnotes of medical books and exotic papers since the initial ...
Paulo Sérgio Gonçalves da Costa, PhD, Geyza Machado Ribeiro, Thiago Cardoso Vale, Thaís Gomes Casali, Flávio José Barbosa Leite   +4 more
doaj   +1 more source