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Antenatal Bartter syndrome.
Afzal M, Khan EA, Khan WA, Anwar V, Yaqoob A, Rafiq S, Azam S. Afzal M, et al. J Coll Physicians Surg Pak. 2014 May;24 Suppl 2:S121-3. J Coll Physicians Surg Pak. 2014. PMID: 24906263
Antenatal Bartter syndrome is characterized by severe polyhydramnios in mother leading to premature delivery. ...
Antenatal Bartter syndrome is characterized by severe polyhydramnios in mother leading to premature delivery. ...
Growth hormone deficiency in children with antenatal Bartter syndrome.
Spector-Cohen I, Koren A, Sakran W, Tenenbaum-Rakover Y, Halevy R. Spector-Cohen I, et al. J Pediatr Endocrinol Metab. 2019 Mar 26;32(3):225-231. doi: 10.1515/jpem-2018-0188. J Pediatr Endocrinol Metab. 2019. PMID: 30844761
The aim of our study was to determine the prevalence of GHD in children with antenatal Bartter syndrome and to assess their response to GH therapy. ...Conclusions In addition to other important causes for poor growth in antenatal Bartter synd …
The aim of our study was to determine the prevalence of GHD in children with antenatal Bartter syndrome and to assess t …
Diagnosis of antenatal Bartter syndrome.
Narayan R, Peres M, Kesby G. Narayan R, et al. Clin Exp Obstet Gynecol. 2016;43(3):453-4. Clin Exp Obstet Gynecol. 2016. PMID: 27328514
Other amniotic fluid biochemical markers have been described, notably increased aldosterone levels, and low total protein levels. NOVEL INSIGHT: Antenatal Bartter syndrome is a heterogeneous group of renal disorders. ...In the setting of unexplained severe po …
Other amniotic fluid biochemical markers have been described, notably increased aldosterone levels, and low total protein levels. NOVEL INSI …
Pharmacotyping of hypokalaemic salt-losing tubular disorders.
Reinalter SC, Jeck N, Peters M, Seyberth HW. Reinalter SC, et al. Acta Physiol Scand. 2004 Aug;181(4):513-21. doi: 10.1111/j.1365-201X.2004.01325.x. Acta Physiol Scand. 2004. PMID: 15283765 Review.
Historically, four phenotypical variants have been described: (1) the (classic) Bartter syndrome (cBS), (2) the hypomagnesaemic hypocalciuric Gitelman syndrome (GS), (3) the hypercalciuric hyperprostaglandin-E-syndrome (HPS) or antenatal Bartter syndrome (aBS …
Historically, four phenotypical variants have been described: (1) the (classic) Bartter syndrome (cBS), (2) the hypomagnesaemic hypocalciuri …
Role of cyclooxygenase-2 in hyperprostaglandin E syndrome/antenatal Bartter syndrome.
Reinalter SC, Jeck N, Brochhausen C, Watzer B, Nüsing RM, Seyberth HW, Kömhoff M. Reinalter SC, et al. Kidney Int. 2002 Jul;62(1):253-60. doi: 10.1046/j.1523-1755.2002.00435.x. Kidney Int. 2002. PMID: 12081585 Free article.
BACKGROUND: Hyperprostaglandin E syndrome/antenatal Bartter syndrome (HPS/aBS) is a congenital salt-losing tubulopathy with an induced expression of cyclooxygenase-2 (COX-2) in the macula densa probably leading to hyperreninemia. ...This observation proves th …
BACKGROUND: Hyperprostaglandin E syndrome/antenatal Bartter syndrome (HPS/aBS) is a congenital salt-losing tubulopathy …
Pathogenetic role of cyclooxygenase-2 in hyperprostaglandin E syndrome/antenatal Bartter syndrome: therapeutic use of the cyclooxygenase-2 inhibitor nimesulide.
Nüsing RM, Reinalter SC, Peters M, Kömhoff M, Seyberth HW. Nüsing RM, et al. Clin Pharmacol Ther. 2001 Oct;70(4):384-90. Clin Pharmacol Ther. 2001. PMID: 11673754 Clinical Trial.
Patients with hyperprostaglandin E syndrome/antenatal Bartter syndrome typically have renal salt wasting, hypercalciuria with nephrocalcinosis, and secondary hyperaldosteronism. Antenatally, these patients have fetal polyuria, leading to polyhydramnios and pr …
Patients with hyperprostaglandin E syndrome/antenatal Bartter syndrome typically have renal salt wasting, hypercalciuri …
The neonatal variant of Bartter syndrome and deafness: preservation of renal function.
Shalev H, Ohali M, Kachko L, Landau D. Shalev H, et al. Pediatrics. 2003 Sep;112(3 Pt 1):628-33. doi: 10.1542/peds.112.3.628. Pediatrics. 2003. PMID: 12949294
BACKGROUND: A subtype of antenatal Bartter syndrome and sensorineural deafness (BSND) was originally described among families from southern Israel, and its gene (Barttin, OMIM #606412) has recently been identified. ...
BACKGROUND: A subtype of antenatal Bartter syndrome and sensorineural deafness (BSND) was originally described among fa …
Hypokalemic salt-losing tubulopathy with chronic renal failure and sensorineural deafness.
Jeck N, Reinalter SC, Henne T, Marg W, Mallmann R, Pasel K, Vollmer M, Klaus G, Leonhardt A, Seyberth HW, Konrad M. Jeck N, et al. Pediatrics. 2001 Jul;108(1):E5. doi: 10.1542/peds.108.1.e5. Pediatrics. 2001. PMID: 11433084
In addition, in 1 kindred, prenatal diagnosis in the second child was established, allowing a prospective clinical evaluation. RESULTS: Clinical presentation of the patients was homogeneous and included premature birth attributable to polyhydramnios, severe renal sa …
In addition, in 1 kindred, prenatal diagnosis in the second child was established, allowing a prospective clinical evaluation. RESULT …
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