Zobrazeno 1 - 10
of 1 583
pro vyhledávání: '"congenital nephrotic syndrome"'
Autor:
Paola Krall, Angélica Rojo, Anita Plaza, Sofia Canals, María Luisa Ceballos, Francisco Cano, José Luis Guerrero
Publikováno v:
Frontiers in Nephrology, Vol 4 (2024)
Externí odkaz:
https://doaj.org/article/7a6dae05ccdc4aaea1ba54373e6087f0
Autor:
Paola Krall, Angélica Rojo, Anita Plaza, Sofia Canals, María Luisa Ceballos, Francisco Cano, José Luis Guerrero
Publikováno v:
Frontiers in Nephrology, Vol 4 (2024)
BackgroundCongenital nephrotic syndrome (CNS) is a severe kidney disorder characterized by edema, massive proteinuria, and hypoalbuminemia that manifests in utero or within three months after birth. CNS affects 1-3 per 100,000 children, primarily ass
Externí odkaz:
https://doaj.org/article/2f56ffd3654f4e21b10167c2f41f8d2b
Autor:
Okko Savonius, Anu Kaskinen, Tuula Hölttä, Elisa Ylinen, Juuso Tainio, Tea Nieminen, Timo Jahnukainen
Publikováno v:
Frontiers in Pediatrics, Vol 12 (2024)
BackgroundPretransplant vaccination is generally recommended to solid organ transplant recipients. In infants with congenital nephrotic syndrome (CNS), the immune response is hypothetically inferior to other patients due to young age and urinary loss
Externí odkaz:
https://doaj.org/article/8c1a33c42afa4ebf8fa6d9f9128dabf0
Autor:
Marc Bosch-Schips, Gonzalo Artaza, Carlos Hernández-Mata, Víctor Pérez Beltrán, Vanessa Cabello Ruiz, Pável Olivera Sumire
Publikováno v:
Frontiers in Pediatrics, Vol 12 (2024)
Direct Oral Anticoagulants (DOACs) typically exhibit a predictable pharmacokinetic and pharmacodynamic response at a fixed dose, not necessitating monitoring under standard conditions. Yet, in specific clinical scenarios that can impair it, like Cong
Externí odkaz:
https://doaj.org/article/de8d0df53c114f5b94bd80ea31a34351
Akademický článek
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Autor:
Arshia Eshtiaghi, Jonathan A. Micieli
Publikováno v:
Case Reports in Nephrology and Dialysis, Vol 12, Iss 1, Pp 57-62 (2022)
Vision loss from nonarteritic anterior ischemic optic neuropathy (NAION) is a rare complication of hemodialysis. Here, we present a case in a young woman and discuss the pathophysiology and implications for the nephrologist. A 24-year-old woman with
Externí odkaz:
https://doaj.org/article/456c85242781449395d2001e5738a94f
Publikováno v:
The Journal of Pediatric Academy, Vol 2, Iss 3, Pp 97-100 (2021)
Introduction: Congenital nephrotic syndrome (CNS) is characterized by severe proteinuria, hypoalbuminemia, and edema within the first three months of life. CNS can occur due to perinatal infections or mutation of genes encoding structural or regulato
Externí odkaz:
https://doaj.org/article/4ca32bb2412848c8ba5f4616ab8814df
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
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Publikováno v:
Taiwanese Journal of Obstetrics & Gynecology, Vol 60, Iss 4, Pp 758-762 (2021)
Objective: To explore the genetic bias in a Chinese family suspected of having congenital nephrotic syndrome of the Finnish type (CNF). Case report: We developed a prenatal genetic diagnosis in a Chinese family with CNF. A single heterozygous mutatio
Externí odkaz:
https://doaj.org/article/45b0877a166c4e9697a1b1f1913cde4b
Publikováno v:
Indian Pediatrics Case Reports, Vol 1, Iss 4, Pp 236-239 (2021)
Background: The term “congenital” is used for cases of nephrotic syndrome (NS) that manifests in the first 3 months of life. They are rare diseases mainly due to genetic causes but sometimes attributed to congenital infections. The prognosis depe
Externí odkaz:
https://doaj.org/article/26d5b4b5551c4ea0a1bf6b087b55d801