Results 71 to 80 of about 2,234 (198)

Coincidence of Polysplenia, Kartagener Syndrome, Dorsal Pancreas Agenesis, and Polycystic Kidney Disease in an Adult

Eurasian Journal of Medicine, 2019
Here we present the case of an adult male patient with the anomalies of polysplenia, Kartagener syndrome, dorsal pancreas agenesis, and adult polycystic kidney disease.
Mustafa Kemal Demir, Yavuz Furuncuoglu
doaj   +1 more source

Kartagener syndrome complicated by immunoglobulin A nephropathy

, 2018
Kentaro Oka,1 Taro Sugase,1 Tetsu Akimoto,1,2 Takuya Murakami,1 Izumi Nagayama,1 Miwa Kaneko,1 Maki Asakura,1 Ken Ohara,1 Osamu Saito,1 Daisuke Nagata1 1Division of Nephrology, Department of Internal Medicine, Jichi Medical University, Tochigi, Japan ...
Ohara K, Kaneko M, Asakura M, Nagata D, Sugase T, Nagayama I, Oka K, Saito O, Murakami T, Akimoto T   +9 more
core  

KARTAGENER SYNDROME

The Professional Medical Journal, 2007
We are reporting a case of Kartagener syndrome in a 19 year old young male, who presented to uswith chronic sinusitis, bronchiectasis and dextrocardia.
KHALID AMIN, MASOOD JAVED, AAMIR HUSAIN, Shahid Abbas, Abid Raza   +4 more
openaire   +2 more sources

Primary ciliary dyskinesia: Kartagener syndrome in a family with a novel DNAH5 gene mutation and variable phenotypes

Egyptian Journal of Medical Human Genetics, 2015
Background: Primary ciliary dyskinesia is a genetically heterogeneous autosomal recessive disorder with variable clinical manifestations, including chronic rhinosinusitis, otitis media, bronchitis, pneumonia, bronchiectasis, situs inversus totalis ...
Makia J. Marafie, Ibrahim S. Al Suliman, Abdullah M. Redha, Abdulrahman M. Alshati   +3 more
doaj   +1 more source

Diagnostic challenges of primary ciliary dyskinesia in adults: clinical case

Известия высших учебных заведений. Поволжский регион: Медицинские науки
Background. In pediatric practice, there exists a rare and difficult-to-diagnose hereditary disorder known as Kartagener syndrome, which is a clinical manifestation of primary ciliary dyskinesia. A classic triad of signs characterizes this disease: situs
Anna A. Dyachkova, Evgeny A. Pudkov
doaj   +1 more source

Actinomyces y síndrome de Kartagener: Reporte de caso y revisión de la literatura

, 2022
Kartagener syndrome, which is part of the subgroup of the primary ciliary dyskinesias, predisposes to recurrent respiratory tract infections due to Haemophilus influenzae, Staphylococcus aureusand Streptococcus pneumoniae.
Rojas Kozhakin, D.V., Guarguati Carrillo, A.A., Martínez Montalvo, Carlos M., Galindo Escucha, C.S., Saumett Lopez, S.V., Pérez Hettinga, M.A., Ordoñez Lopez, H.E.   +6 more
core  

New Treatments Are Urgently Needed for Patients With All Primary Ciliary Dyskinesia Genotypes

Pediatric Pulmonology, Volume 60, Issue 11, November 2025.
Benjamin Gaston, Amjad Horani, Stephanie Davis, Thomas Ferkol, BreAnna Kinghorn, Margaret Rosenfeld, Adam Shapiro, Evans Machogu, Michael O'Connor, Harriet Holme, Michele Manion   +10 more
wiley   +1 more source

A case of Kartagener syndrome with rhinolalia clausa [PDF]

, 2016
Kartagener syndrome is an autosomal recessive genetic ciliary disorder comprising of a classic triad of sinusitis, situs inversus and bronchiectasis. It's the one of primary ciliary dyskinesia disorders with manifestations present from childhood.
Elouazzani, Hanane, Rhorfi, Ismail Abderrahmane, Abid, Ahmed, Sator, Hicham, Lahma, Jawad, El Ayoubi, Ali, Benbouzid, Mohammed Anas, Essakalli, Leila, Nitassi, Sophia, Raoufi, Mohammed, Oujilal, Abdelilah   +10 more
core   +1 more source

Síndrome de Kartagener (Discinecia Ciliar Primaria) Presentación de Caso

Cedamaz, 2017
El síndrome de Kartagener es un trastorno hereditario, autosómico, recesivo y de baja frecuencia. Considerándose una variante clínica de la discinecia ciliar primaria.
Luis Aguirre, Gabriela Criollo, Luis Ordoñez, Carlos Rojas, Franklin Padilla   +4 more
doaj  

Kartagener syndrome with pulmonary tuberculosis in a fertile male: A rare co-existence

Journal of Medical Sciences, 2015
Kartagener syndrome (KS), a subset of primary ciliary dyskinesia, is an autosomal recessive disorder with variable phenotypic expressions. Males with this syndrome are usually infertile.
Manoj Kumar Panigrahi, King Herald Kisku
doaj   +1 more source