{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,6,16]],"date-time":"2026-06-16T02:55:05Z","timestamp":1781578505747,"version":"3.54.5"},"reference-count":34,"publisher":"Springer Science and Business Media LLC","issue":"4","license":[{"start":{"date-parts":[[2017,3,10]],"date-time":"2017-03-10T00:00:00Z","timestamp":1489104000000},"content-version":"unspecified","delay-in-days":0,"URL":"http:\/\/www.springer.com\/tdm"}],"content-domain":{"domain":["link.springer.com"],"crossmark-restriction":false},"short-container-title":["Arch Gynecol Obstet"],"published-print":{"date-parts":[[2017,4]]},"DOI":"10.1007\/s00404-017-4336-6","type":"journal-article","created":{"date-parts":[[2017,3,10]],"date-time":"2017-03-10T08:46:47Z","timestamp":1489135607000},"page":"897-906","update-policy":"https:\/\/doi.org\/10.1007\/springer_crossmark_policy","source":"Crossref","is-referenced-by-count":31,"title":["Prenatal ultrasound, genotype, and outcome in a large cohort of prenatally affected patients with autosomal-recessive polycystic kidney disease and other hereditary cystic kidney diseases"],"prefix":"10.1007","volume":"295","author":[{"given":"Florian","family":"Erger","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Nadina Ortiz","family":"Br\u00fcchle","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Ulrich","family":"Gembruch","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Klaus","family":"Zerres","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"297","published-online":{"date-parts":[[2017,3,10]]},"reference":[{"key":"4336_CR1","doi-asserted-by":"crossref","unstructured":"Grijseels EW, van-Hornstra PT, Govaerts LC, Cohen-Overbeek TE, de Krijger RR, Smit BJ, Cransberg K (2011) Outcome of pregnancies complicated by oligohydramnios or anhydramnios of renal origin. Prenat Diagn 31:1039\u20131045","DOI":"10.1002\/pd.2827"},{"issue":"2","key":"4336_CR2","doi-asserted-by":"crossref","first-page":"327","DOI":"10.1007\/s00404-015-3648-7","volume":"292","author":"JE Spiro","year":"2015","unstructured":"Spiro JE, Konrad M, Rieger-Fackeldey E, Masjosthusmann K, Amler S, Klockenbusch W, Schmitz R (2015) Renal oligo- and anhydramnios: cause, course and outcome\u2014a single-center study. Arch Gynecol Obstet 292(2):327\u2013336","journal-title":"Arch Gynecol Obstet"},{"key":"4336_CR3","doi-asserted-by":"crossref","first-page":"68","DOI":"10.1016\/S0022-3476(46)80241-5","volume":"29","author":"EL Potter","year":"1946","unstructured":"Potter EL (1946) Bilateral renal agenesis. J Pediatr 29:68\u201376","journal-title":"J Pediatr"},{"key":"4336_CR4","doi-asserted-by":"crossref","first-page":"303","DOI":"10.1007\/s001090050221","volume":"76","author":"K Zerres","year":"1998","unstructured":"Zerres K, Rudnik-Sch\u00f6neborn S, Steinkamm C, Becker J, M\u00fccher G (1998) Autosomal recessive polycystic kidney disease. J Mol Med (Berl) 76:303\u2013309","journal-title":"J Mol Med (Berl)"},{"key":"4336_CR5","doi-asserted-by":"crossref","first-page":"453","DOI":"10.1002\/humu.20029","volume":"23","author":"C Bergmann","year":"2004","unstructured":"Bergmann C, Senderek J, K\u00fcpper F, Schneider F, Dornia C, Windelen E, Eggermann T, Rudnik-Sch\u00f6neborn S, Kirfel J, Furu L, Onuchic LF, Rossetti S, Harris PC, Somlo S, Guay-Woodford L, Germino GG, Moser M, B\u00fcttner R, Zerres K (2004) PKHD1 mutations in autosomal recessive polycystic kidney disease (ARPKD). Hum Mutat 23:453\u2013463","journal-title":"Hum Mutat"},{"key":"4336_CR6","doi-asserted-by":"crossref","first-page":"148","DOI":"10.1038\/pr.2013.191","volume":"75","author":"WE Sweeney Jr","year":"2014","unstructured":"Sweeney WE Jr, Avner ED (2014) Pathophysiology of childhood polycystic kidney diseases: new insights into disease-specific therapy. Pediatr Res 75:148\u2013157","journal-title":"Pediatr Res"},{"key":"4336_CR7","doi-asserted-by":"crossref","first-page":"829","DOI":"10.1111\/j.1523-1755.2005.00148.x","volume":"67","author":"C Bergmann","year":"2005","unstructured":"Bergmann C, Senderek J, Windelen E, K\u00fcpper F, Middeldorf I, Schneider F, Dornia C, Rudnik-Sch\u00f6neborn S, Konrad M, Schmitt CP, Seeman T, Neuhaus TJ, Vester U, Kirfel J, B\u00fcttner R, Zerres K, APN (Arbeitsgemeinschaft f\u00fcr P\u00e4diatrische Nephrologie) (2005) Clinical consequences of PKHD1 mutations in 164 patients with autosomal-recessive polycystic kidney disease (ARPKD). Kidney Int 67:829\u2013848","journal-title":"Kidney Int"},{"key":"4336_CR8","doi-asserted-by":"crossref","first-page":"1004","DOI":"10.2214\/AJR.11.8083","volume":"198","author":"FE Avni","year":"2012","unstructured":"Avni FE, Garel C, Cassart M, D\u2019Haene N, Hall M, Riccabona M (2012) Imaging and classification of congenital cystic renal diseases. Am J Roentgenol 198:1004\u20131013","journal-title":"Am J Roentgenol"},{"key":"4336_CR9","doi-asserted-by":"crossref","first-page":"911","DOI":"10.1002\/uog.3856","volume":"28","author":"K Chaumoitre","year":"2006","unstructured":"Chaumoitre K, Brun M, Cassart M, Maugey-Laulom B, Eurin D, Didier F, Avni EF (2006) Differential diagnosis of fetal hyperechogenic cystic kidneys unrelated to renal tract anomalies: a multicenter study. Ultrasound Obstet Gynecol 28:911\u2013917","journal-title":"Ultrasound Obstet Gynecol"},{"key":"4336_CR10","doi-asserted-by":"crossref","first-page":"154","DOI":"10.4103\/1817-1745.117855","volume":"8","author":"SV Parelkar","year":"2013","unstructured":"Parelkar SV, Kapadnis SP, Sanghvi BV, Joshi PB, Mundada D, Oak SN (2013) Meckel-Gruber syndrome: a rare and lethal anomaly with review of literature. J Pediatr Neurosci. 8:154\u2013157","journal-title":"J Pediatr Neurosci."},{"key":"4336_CR11","doi-asserted-by":"crossref","first-page":"296","DOI":"10.1002\/uog.2708","volume":"27","author":"V Ickowicz","year":"2006","unstructured":"Ickowicz V, Eurin D, Maugey-Laulom B, Didier F, Garel C, Gubler MC, Laquerri\u00e8re A, Avni EF (2006) Meckel-Gruber syndrome: sonography and pathology. Ultrasound Obstet Gynecol 27:296\u2013300","journal-title":"Ultrasound Obstet Gynecol"},{"key":"4336_CR12","doi-asserted-by":"crossref","first-page":"889","DOI":"10.1016\/j.pcl.2006.08.012","volume":"53","author":"ED Avner","year":"2006","unstructured":"Avner ED, Sweeney WE Jr (2006) Renal cystic disease: new insights for the clinician. Pediatr Clin North Am 53:889\u2013909","journal-title":"Pediatr Clin North Am"},{"key":"4336_CR13","doi-asserted-by":"crossref","unstructured":"Zerres K, Rudnik-Sch\u00f6neborn S, Deget F, and members of the German working group on paediatric nephrology (Arbeitsgemeinschaft f\u00fcr P\u00e4diatrische Nephrologie) (1993) Childhood onset autosomal dominant polycystic kidney disease in sibs: clinical picture and recurrence risk. J Med Genet 30:583\u2013588","DOI":"10.1136\/jmg.30.7.583"},{"key":"4336_CR14","doi-asserted-by":"crossref","first-page":"13","DOI":"10.1136\/jmg.35.1.13","volume":"35","author":"KD MacDermot","year":"1998","unstructured":"MacDermot KD, Saggar-Malik AK, Economides DL, Jeffery S (1998) Prenatal diagnosis of autosomal dominant polycystic kidney disease (PKD1) presenting in utero and prognosis for very early onset disease. J Med Genet 35:13\u201316","journal-title":"J Med Genet"},{"key":"4336_CR15","doi-asserted-by":"crossref","first-page":"380","DOI":"10.1007\/s00467-006-0327-8","volume":"22","author":"O Boyer","year":"2007","unstructured":"Boyer O, Gagnadoux MF, Guest G, Biebuyck N, Charbit M, Salomon R, Niaudet P (2007) Prognosis of autosomal dominant polycystic kidney disease diagnosed in utero or at birth. Pediatr Nephrol 22:380\u2013388","journal-title":"Pediatr Nephrol"},{"key":"4336_CR16","doi-asserted-by":"crossref","first-page":"2047","DOI":"10.1681\/ASN.2010101080","volume":"22","author":"C Bergmann","year":"2011","unstructured":"Bergmann C, von Bothmer J, Ortiz Br\u00fcchle N, Venghaus A, Frank V, Fehrenbach H, Hampel T, Pape L, Buske A, Jonsson J, Sarioglu N, Santos A, Ferreira JC, Becker JU, Cremer R, Hoefele J, Benz MR, Weber LT, Buettner R, Zerres K (2011) Mutations in multiple PKD genes may explain early and severe polycystic kidney disease. J Am Soc Nephrol 22:2047\u20132056","journal-title":"J Am Soc Nephrol"},{"key":"4336_CR17","doi-asserted-by":"crossref","first-page":"55","DOI":"10.1002\/uog.1098","volume":"24","author":"M Brun","year":"2004","unstructured":"Brun M, Maugey-Laulom B, Eurin D, Didier F, Avni EF (2004) Prenatal sonographic patterns in autosomal dominant polycystic kidney disease: a multicenter study. Ultrasound Obstet Gynecol 24:55\u201361","journal-title":"Ultrasound Obstet Gynecol"},{"key":"4336_CR18","doi-asserted-by":"crossref","first-page":"1042","DOI":"10.1053\/j.ajkd.2008.05.015","volume":"52","author":"B Reed","year":"2008","unstructured":"Reed B, McFann K, Kimberling WJ, Pei Y, Gabow PA, Christopher K, Petersen E, Kelleher C, Fain PR, Johnson A, Schrier RW (2008) Presence of de novo mutations in autosomal dominant polycystic kidney disease patients without family history. Am J Kidney Dis 52:1042\u20131050","journal-title":"Am J Kidney Dis"},{"key":"4336_CR19","unstructured":"Harris PC, Torres VE. Polycystic Kidney Disease, Autosomal Dominant. In: Pagon RA, Adam MP, Bird TD, Dolan CR, Fong CT, Stephens K, editors. GeneReviews\u2122 [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2013. 2002 Jan 10 [updated 2011 Dec 08]. Available at http:\/\/www.ncbi.nlm.nih.gov\/books\/NBK1246"},{"key":"4336_CR20","doi-asserted-by":"crossref","first-page":"84","DOI":"10.1136\/jmg.2005.032854","volume":"43","author":"EL Edghill","year":"2006","unstructured":"Edghill EL, Bingham C, Ellard S, Hattersley AT (2006) Mutations in hepatocyte nuclear factor-1beta and their related phenotypes. J Med Genet 43:84\u201390","journal-title":"J Med Genet"},{"key":"4336_CR21","doi-asserted-by":"crossref","first-page":"248","DOI":"10.1038\/nmeth0410-248","volume":"7","author":"IA Adzhubei","year":"2010","unstructured":"Adzhubei IA, Schmidt S, Peshkin L, Ramensky VE, Gerasimova A, Bork P, Kondrashov AS, Sunyaev SR (2010) A method and server for predicting damaging missense mutations. Nat Methods 7:248\u2013249","journal-title":"Nat Methods"},{"key":"4336_CR22","doi-asserted-by":"crossref","first-page":"104","DOI":"10.1007\/BF00279301","volume":"68","author":"K Zerres","year":"1984","unstructured":"Zerres K, V\u00f6lpel MC, Weiss H (1984) Cystic kidneys. Genetics, pathologic anatomy, clinical picture, and prenatal diagnosis. Hum Genet 68:104\u2013135","journal-title":"Hum Genet"},{"key":"4336_CR23","doi-asserted-by":"crossref","first-page":"197","DOI":"10.3109\/00016349009028681","volume":"69","author":"P Bergsj\u00f8","year":"1990","unstructured":"Bergsj\u00f8 P, Denman DW 3rd, Hoffman HJ, Meirik O (1990) Duration of human singleton pregnancy. A population-based study. Acta Obstet Gynecol Scand 69:197\u2013207","journal-title":"Acta Obstet Gynecol Scand"},{"key":"4336_CR24","doi-asserted-by":"crossref","first-page":"391","DOI":"10.1046\/j.1523-1755.2003.00111.x","volume":"64","author":"S Rossetti","year":"2003","unstructured":"Rossetti S, Torra R, Coto E, Consugar M, Kubly V, M\u00e1laga S, Navarro M, El-Youssef M, Torres VE, Harris PC (2003) A complete mutation screen of PKHD1 in autosomal-recessive polycystic kidney disease (ARPKD) pedigrees. Kidney Int 64:391\u2013403","journal-title":"Kidney Int"},{"key":"4336_CR25","doi-asserted-by":"crossref","first-page":"1072","DOI":"10.1542\/peds.111.5.1072","volume":"111","author":"LM Guay-Woodford","year":"2003","unstructured":"Guay-Woodford LM, Desmond RA (2003) Autosomal recessive polycystic kidney disease: the clinical experience in North America. Pediatrics 111:1072\u20131080","journal-title":"Pediatrics"},{"key":"4336_CR26","doi-asserted-by":"crossref","first-page":"316","DOI":"10.1016\/S0002-9378(97)70491-5","volume":"176","author":"W Sepulveda","year":"1997","unstructured":"Sepulveda W, Sebire NJ, Souka A, Snijders RJ, Nicolaides KH (1997) Diagnosis of the Meckel-Gruber syndrome at eleven to fourteen weeks\u2019 gestation. Am J Obstet Gynecol 176:316\u2013319","journal-title":"Am J Obstet Gynecol"},{"key":"4336_CR27","doi-asserted-by":"crossref","first-page":"432","DOI":"10.1093\/ndt\/gfl591","volume":"22","author":"I Klaassen","year":"2007","unstructured":"Klaassen I, Neuhaus TJ, Mueller-Wiefel DE, Kemper MJ (2007) Antenatal oligohydramnios of renal origin: long-term outcome. Nephrol Dial Transplant 22:432\u2013439","journal-title":"Nephrol Dial Transplant"},{"key":"4336_CR28","first-page":"322","volume":"22","author":"N Ortiz Br\u00fcchle","year":"2010","unstructured":"Ortiz Br\u00fcchle N, Venghaus A, von Bothmer J, Rudnik-Schoneborn S, Eggermann T, Bergmann C, Zerres K (2010) Cystic kidney diseases: an overview. Med Genet 22:322\u2013331","journal-title":"Med Genet"},{"key":"4336_CR29","doi-asserted-by":"crossref","first-page":"250","DOI":"10.1542\/peds.109.2.250","volume":"109","author":"JA Laudy","year":"2002","unstructured":"Laudy JA, Tibboel D, Robben SG, de Krijger RR, de Ridder MA, Wladimiroff JW (2002) Prenatal prediction of pulmonary hypoplasia: clinical, biometric, and Doppler velocity correlates. Pediatrics 109:250\u2013258","journal-title":"Pediatrics"},{"key":"4336_CR30","doi-asserted-by":"crossref","first-page":"215","DOI":"10.1002\/pd.1970080308","volume":"8","author":"K Zerres","year":"1988","unstructured":"Zerres K, Hansmann M, Mallmann R, Gembruch U (1988) Autosomal recessive polycystic kidney disease. Problems of prenatal diagnosis. Prenat Diagn 8:215\u2013229","journal-title":"Prenat Diagn."},{"key":"4336_CR31","doi-asserted-by":"crossref","first-page":"923","DOI":"10.1681\/ASN.2006091057","volume":"18","author":"S Decramer","year":"2007","unstructured":"Decramer S, Parant O, Beaufils S, Clauin S, Guillou C, Kessler S, Aziza J, Bandin F, Schanstra JP, Bellann\u00e9-Chantelot C (2007) Anomalies of the TCF2 gene are the main cause of fetal bilateral hyperechogenic kidneys. J Am Soc Nephrol 18:923\u2013933","journal-title":"J Am Soc Nephrol"},{"key":"4336_CR32","doi-asserted-by":"crossref","first-page":"1388","DOI":"10.1046\/j.1471-0528.2002.02055.x","volume":"109","author":"V Tsatsaris","year":"2002","unstructured":"Tsatsaris V, Gagnadoux MF, Aubry MC, Gubler MC, Dumez Y, Dommergues M (2002) Prenatal diagnosis of bilateral isolated fetal hyperechogenic kidneys. Is it possible to predict long term outcome? BJOG 109:1388\u20131393","journal-title":"BJOG"},{"key":"4336_CR33","doi-asserted-by":"crossref","first-page":"637","DOI":"10.1016\/j.jgyn.2010.07.012","volume":"39","author":"V Emmanuelli","year":"2010","unstructured":"Emmanuelli V, Lahoche-Manucci A, Holder-Espinasse M, Devisme L, Vaast P, Dieux-Coeslier A, Dehennault M, Petit S, Besson R, Houfflin-Debarge V (2010) Prenatal diagnosis of hyperechogenic kidneys: a study of 17 cases. J Gynecol Obstet Biol Reprod (Paris). 39:637\u2013646","journal-title":"J Gynecol Obstet Biol Reprod (Paris)."},{"key":"4336_CR34","doi-asserted-by":"crossref","first-page":"1429","DOI":"10.1148\/rg.226025047","volume":"22","author":"MG Mercado-Deane","year":"2002","unstructured":"Mercado-Deane MG, Beeson JE, John SD (2002) US of renal insufficiency in neonates. Radiographics 22:1429\u20131438","journal-title":"Radiographics"}],"container-title":["Archives of Gynecology and Obstetrics"],"original-title":[],"language":"en","link":[{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/s00404-017-4336-6.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/article\/10.1007\/s00404-017-4336-6\/fulltext.html","content-type":"text\/html","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/s00404-017-4336-6.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2017,6,25]],"date-time":"2017-06-25T12:21:52Z","timestamp":1498393312000},"score":1,"resource":{"primary":{"URL":"http:\/\/link.springer.com\/10.1007\/s00404-017-4336-6"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2017,3,10]]},"references-count":34,"journal-issue":{"issue":"4","published-print":{"date-parts":[[2017,4]]}},"alternative-id":["4336"],"URL":"https:\/\/doi.org\/10.1007\/s00404-017-4336-6","relation":{},"ISSN":["0932-0067","1432-0711"],"issn-type":[{"value":"0932-0067","type":"print"},{"value":"1432-0711","type":"electronic"}],"subject":[],"published":{"date-parts":[[2017,3,10]]}}}