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Year Number of Results
1984 1
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1991 2
1992 5
1993 4
1994 4
1995 6
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1997 14
1998 10
1999 5
2000 10
2001 6
2002 4
2003 6
2004 6
2005 5
2006 13
2007 6
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2009 11
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278 results

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Page 1
Chronic abruption-oligohydramnios sequence.
Elliott JP, Gilpin B, Strong TH Jr, Finberg HJ. Elliott JP, et al. J Reprod Med. 1998 May;43(5):418-22. J Reprod Med. 1998. PMID: 9610464
All patients with a diagnosis of placental abruption with oligohydramnios or ruptured membranes were included. Chronic abruption-oligohydramnios sequence (CAOS) was defined by the following criteria: (1) clinically significant vaginal bleeding in the absence …
All patients with a diagnosis of placental abruption with oligohydramnios or ruptured membranes were included. Chronic abruption-o …
Chronic abruption-oligohydramnios sequence (CAOS) revisited: possible implication of premature rupture of membranes.
Chigusa Y, Mogami H, Minamiguchi S, Kido A, Ishida A, Kurata Y, Yasuda E, Kawasaki K, Horie A, Yamaguchi K, Mandai M, Kondoh E. Chigusa Y, et al. J Matern Fetal Neonatal Med. 2022 Dec;35(25):6894-6900. doi: 10.1080/14767058.2021.1929159. Epub 2021 May 20. J Matern Fetal Neonatal Med. 2022. PMID: 34016009
AIM: The pathogenic mechanism of chronic abruption-oligohydramnios sequence (CAOS) remains unknown, and there are no objective standards for diagnosis on imaging or using pathological evidence. ...
AIM: The pathogenic mechanism of chronic abruption-oligohydramnios sequence (CAOS) remains unknown, and there are no objective …
Potter Syndrome.
Bhandari J, Thada PK, Sergent SR. Bhandari J, et al. 2023 Aug 8. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2024 Jan–. 2023 Aug 8. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2024 Jan–. PMID: 32809693 Free Books & Documents.
Potter sequence and Potter syndrome are used interchangeably because the sequence of events leading to oligohydramnios is consistent. But the Potter sequence more specifically describes the decreased amniotic fluid irrespective of the cause. ...
Potter sequence and Potter syndrome are used interchangeably because the sequence of events leading to oligohydramnios …
Oligohydramnios sequence revisited in relationship to arthrogryposis, with distinctive skin changes.
Hall JG. Hall JG. Am J Med Genet A. 2014 Nov;164A(11):2775-92. doi: 10.1002/ajmg.a.36731. Epub 2014 Aug 26. Am J Med Genet A. 2014. PMID: 25160497
Thirty cases of arthrogryposis associated with longstanding oligohydramnios were identified among 2,500 cases of arthrogryposis (1.2%) and were reviewed for clinical features and natural history. ...Sixty percent (18/30) seemed to have their multiple congenital contracture …
Thirty cases of arthrogryposis associated with longstanding oligohydramnios were identified among 2,500 cases of arthrogryposis (1.2% …
Decrease of the incidence of renin-angiotensin-system inhibitor induced oligohydramnios-sequence in Germany in 2011.
Hünseler C, von Kries R, Roth B. Hünseler C, et al. Klin Padiatr. 2014 Apr;226(2):59-61. doi: 10.1055/s-0033-1363267. Epub 2014 Mar 14. Klin Padiatr. 2014. PMID: 24633976 Review.
AIM: to assess whether the incidence of angiotensin II-receptor type 1 antagonist (AT1-antagonist)- or ACE-inhibitor induced cases of oligohydramnios sequence (OHS) in 2011 was reduced after intensive alerts as to the causal association between AT1-antagonist /ACE-i …
AIM: to assess whether the incidence of angiotensin II-receptor type 1 antagonist (AT1-antagonist)- or ACE-inhibitor induced cases of oli …
Limb deformations in oligohydramnios sequence: effects of gestational age and duration of oligohydramnios.
Christianson C, Huff D, McPherson E. Christianson C, et al. Am J Med Genet. 1999 Oct 29;86(5):430-3. Am J Med Genet. 1999. PMID: 10508984
Clubfoot was the most frequent at all ages, but hand contractures such as camptodactyly were common only in the 2nd trimester while the broad flat hand originally described in Potter sequence was found almost exclusively in the fetuses with oligohydramnios in the 3r …
Clubfoot was the most frequent at all ages, but hand contractures such as camptodactyly were common only in the 2nd trimester while the broa …
Prune Belly Syndrome.
Pomajzl AJ, Sankararaman S. Pomajzl AJ, et al. 2023 Aug 8. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2024 Jan–. 2023 Aug 8. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2024 Jan–. PMID: 31334968 Free Books & Documents.
Perinatal mortality ranges between 10 to 25% in contemporary studies and directly correlates to the severity of pulmonary hypoplasia as a result of oligohydramnios from reduced fetal urine production from renal dysplasia and urinary tract abnormalities leading to Potter …
Perinatal mortality ranges between 10 to 25% in contemporary studies and directly correlates to the severity of pulmonary hypoplasia as a re …
Twin Anemia-Polycythemia Sequence (TAPS): From Basic Research to Clinical Practice.
da Silva Rocha J, Guedes-Martins L, Cunha A. da Silva Rocha J, et al. Curr Vasc Pharmacol. 2023;21(2):91-105. doi: 10.2174/1570161121666230131112930. Curr Vasc Pharmacol. 2023. PMID: 36718965 Review.
In monochorionic (MC) pregnancies, the fetuses share the same placental mass and exhibit vascular anastomoses crossing the intertwin membrane, and the combination and pattern of anastomoses determine the primary clinical picture and occurrence of future complications. Twin Anemia …
In monochorionic (MC) pregnancies, the fetuses share the same placental mass and exhibit vascular anastomoses crossing the intertwin membran …
Renal tubular dysgenesis.
Gubler MC. Gubler MC. Pediatr Nephrol. 2014 Jan;29(1):51-9. doi: 10.1007/s00467-013-2480-1. Epub 2013 May 1. Pediatr Nephrol. 2014. PMID: 23636579 Review.
Renal tubular dysgenesis (RTD) is a severe foetal disorder characterised by the absence or poor development of proximal tubules, early onset and persistent anuria (leading to oligohydramnios and the Potter sequence) and ossification defects of the skull. ...
Renal tubular dysgenesis (RTD) is a severe foetal disorder characterised by the absence or poor development of proximal tubules, early onset …
Clinical utility of chromosomal microarray analysis and whole exome sequencing in foetuses with oligohydramnios.
Shi X, Ding H, Li C, Liu L, Yu L, Zhu J, Wu J. Shi X, et al. Ann Med. 2023 Dec;55(1):2215539. doi: 10.1080/07853890.2023.2215539. Ann Med. 2023. PMID: 37243546 Free PMC article.
OBJECTIVES: To evaluate the clinical utility of chromosomal microarray analysis (CMA) and whole exome sequencing (WES) in foetuses with oligohydramnios. ...WES should be recommended for fetuses with oligohydramnios. CMA has low diagnostic utility for …
OBJECTIVES: To evaluate the clinical utility of chromosomal microarray analysis (CMA) and whole exome sequencing (WES) in foet …
278 results