Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Fetal polyuria"'
Publikováno v:
J Pediatr Genet
Bartter's disease, an inherited renal tubular disorder is due to a defect in ion transport across the ascending limb of the loop of Henle leading to failure of the ability of kidneys to concentrate urine and hence polyuria. We present three fetuses o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5164dbfa6ceb8e9889556271e2526b8f
https://doi.org/10.1055/s-0040-1713157
https://doi.org/10.1055/s-0040-1713157
Publikováno v:
Revista chilena de pediatría v.90 n.4 2019
SciELO Chile
CONICYT Chile
instacron:CONICYT
SciELO Chile
CONICYT Chile
instacron:CONICYT
Introduction: Bartter syndrome (BS) is a rare inherited tubulopathy that has two presentation forms, the first one is a severe form of antenatal onset (neonatal Bartter) and the second one is a later onset form during the first years of life (classic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::50aaa30d2ed98a47accf5ddaeb86b60a
http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0370-41062019000400437
http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0370-41062019000400437
Autor:
Rosa Vargas-Poussou, Isabelle Czerkiewicz, Dominique Mahieu-Caputo, Myriam Rachid, Jean-François Oury, Georges Deschênes, Sophie Dreux, Françoise Muller
Publikováno v:
Clinical Case Reports
Bartter syndrome is a severe inherited tubulopathy responsible for renal salt wasting. It is caused by alterations in ion channels located in the thick ascending limb of Henle's loop. Five mutations in four genes – SLC12A1, KCNJ1, CLCNKB, and BSND
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4d12cd249ee3bba57909ae52eabc616e
http://europepmc.org/articles/PMC5018593
http://europepmc.org/articles/PMC5018593
Autor:
Robert A. Brace, Ralph W Thurlow
Publikováno v:
American Journal of Obstetrics and Gynecology. 189:601-608
Four days of hypoxia produce an extensive fetal polyuria with little change in amniotic fluid volume in the ovine fetus. We hypothesized that fetal swallowing and intramembranous absorption would increase with prolonged hypoxia to offset the polyuria
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e409b469141bf7ac02499c51f5c09261
https://doi.org/10.1067/s0002-9378(03)00494-0
https://doi.org/10.1067/s0002-9378(03)00494-0
Publikováno v:
Obstetrics & Gynecology. 116:547-549
BACKGROUND: Diabetes insipidus is rare in pregnancy. It is characterized by hypoosmolar polyuria and may be central, nephrogenic, or transient in etiology; the latter is presumably related to excess placental vasopresinase production. In theory, feta
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ad26e1ffdf4553782c2267458773cdcc
https://doi.org/10.1097/aog.0b013e3181e6c683
https://doi.org/10.1097/aog.0b013e3181e6c683
Publikováno v:
International Journal of Pediatrics
International Journal of Pediatrics, Vol 2012 (2012)
International Journal of Pediatrics, Vol 2012 (2012)
Antenatal Bartter syndrome (ABS) is a rare autosomal recessive renal tubular disorder. The defective chloride transport in the loop of Henle leads to fetal polyuria resulting in severe hydramnios and premature delivery. Early onset, unexplained mater
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e8927d02c635e2c797e2a52ca61d19d0
http://europepmc.org/articles/PMC3299276
http://europepmc.org/articles/PMC3299276
Publikováno v:
The Journal of Pediatrics. 120:129-132
After a pregnancy complicated by severe hydramnios, a preterm infant had clinical and biochemical evidence of pseudohypoaldosteronism. Fetal polyuria probably caused the hydramnios.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0ec9d6bddab7ceb7c70bb2a30852c89d
https://doi.org/10.1016/s0022-3476(05)80617-1
https://doi.org/10.1016/s0022-3476(05)80617-1
Autor:
Arnaud Garnier, Sophie Dreux, Jean-François Oury, Alexandra Benachi, Georges Deschênes, Françoise Muller, Rosa Vargas-Poussou
Publikováno v:
Pediatric research. 67(3)
Bartter syndrome is an autosomic recessive disease characterized by severe polyuria and sodium renal loss. The responsible genes encode proteins involved in electrolyte tubular reabsorption. Prenatal manifestations, mainly recurrent polyhydramnios be
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5ab03a15eaaf5b5aea1a1f28e60f158e
https://pubmed.ncbi.nlm.nih.gov/19915517
https://pubmed.ncbi.nlm.nih.gov/19915517
Publikováno v:
Fetal diagnosis and therapy. 22(3)
Antenatal Bartter syndrome typically presents with marked fetal polyuria that leads to polyhydramnios and premature delivery. In our case, polyhydramnios was detected at 26 weeks of gestation and amniotic fluid chloride level was high. Serial amnion-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3da88b5a91938765772d3a7bc9731c6a
https://pubmed.ncbi.nlm.nih.gov/17228161
https://pubmed.ncbi.nlm.nih.gov/17228161
Publisher Summary The combination of autosomal recessively transmitted hypokalemic alkalosis and normotensive hyperalsosteronism is termed as Bartter syndrome. Three main phenotypical variants of this syndrome are described in this chapter: the class
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f6fb37f41c2b1b77f271ddfa3b50398d
https://doi.org/10.1016/b978-044450489-0/50015-x
https://doi.org/10.1016/b978-044450489-0/50015-x