{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,7]],"date-time":"2026-10-07T02:52:05Z","timestamp":1791341525421,"version":"4.3.1"},"reference-count":15,"publisher":"Wiley","issue":"7","license":[{"start":{"date-parts":[[2009,5,27]],"date-time":"2009-05-27T00:00:00Z","timestamp":1243382400000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["J of Clinical Ultrasound"],"published-print":{"date-parts":[[2009,9]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:p>Short rib polydactyly syndrome (SRPS) is a very rare congenital autosomal recessive inherited disease, classified into four subtypes. It has distinct imaging findings on prenatal sonography (US) and ancillary findings on both pre\u2010 and postnatal examinations may help classify individual cases into one of four subtypes. We report the US findings in a case of SRPS type IV (Beemer\u2013Langer dysplasia) in a male fetus with multiple congenital anomalies, including cystic hygroma. The postnatal ultrasound, radiographic, and postmortem examinations helped to classify the SRPS as type IV. We believe this is the first documented case associating cystic hygroma and polydactyly. \u00a9 2009 Wiley Periodicals, Inc. J Clin Ultrasound 2009<\/jats:p>","DOI":"10.1002\/jcu.20603","type":"journal-article","created":{"date-parts":[[2009,5,28]],"date-time":"2009-05-28T00:20:42Z","timestamp":1243470042000},"page":"406-409","source":"Crossref","is-referenced-by-count":5,"title":["Diagnosis of short rib polydactyly syndrome type IV (Beemer\u2013Langer syndrome) with cystic hygroma: A case report"],"prefix":"10.1002","volume":"37","author":[{"given":"Kishor B.","family":"Taori","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Kedar G.","family":"Sharbidre","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Vijay","family":"Krishnan","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Nischal","family":"Kundargi","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Bipin R.","family":"Kulkarni","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Vinay","family":"Satkar","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Sneha","family":"Bopche","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"311","published-online":{"date-parts":[[2009,5,27]]},"reference":[{"key":"e_1_2_1_2_2","first-page":"80","article-title":"Short\u2010rib\u2010polydactyly syndrome type Verma\u2010Naumoff\u2010Le Marec in a fetus with histological hallmarks of type Saldino\u2010Noonan but lacking internal organ abnormalities","volume":"16","author":"Hentze S","year":"1998","journal-title":"Am J Med Genet"},{"key":"e_1_2_1_3_2","first-page":"1192","volume-title":"Textbook of fetal and perinatal pathology","author":"Yang SS","year":"1991"},{"key":"e_1_2_1_4_2","doi-asserted-by":"publisher","DOI":"10.1016\/S0301-2115(99)00161-X"},{"key":"e_1_2_1_5_2","doi-asserted-by":"publisher","DOI":"10.1002\/ajmg.10562"},{"key":"e_1_2_1_6_2","doi-asserted-by":"publisher","DOI":"10.2214\/ajr.114.2.257"},{"key":"e_1_2_1_7_2","doi-asserted-by":"publisher","DOI":"10.1148\/radiology.144.3.7100463"},{"key":"e_1_2_1_8_2","doi-asserted-by":"publisher","DOI":"10.1002\/ajmg.1320140307"},{"key":"e_1_2_1_9_2","doi-asserted-by":"publisher","DOI":"10.1136\/jmg.19.2.141"},{"key":"e_1_2_1_10_2","doi-asserted-by":"publisher","DOI":"10.1288\/00005537-199006000-00005"},{"key":"e_1_2_1_11_2","doi-asserted-by":"publisher","DOI":"10.1159\/000086822"},{"key":"e_1_2_1_12_2","doi-asserted-by":"publisher","DOI":"10.1002\/ajmg.1320140116"},{"key":"e_1_2_1_13_2","doi-asserted-by":"publisher","DOI":"10.1111\/j.1399-0004.1991.tb03029.x"},{"key":"e_1_2_1_14_2","doi-asserted-by":"publisher","DOI":"10.1136\/adc.15.82.65"},{"key":"e_1_2_1_15_2","doi-asserted-by":"publisher","DOI":"10.1002\/ajmg.1320210304"},{"key":"e_1_2_1_16_2","first-page":"461","article-title":"Complex consanguinity associated with short rib\u2010polydactyly syndrome III and congenital infection\u2010like syndrome: a diagnostic problem in dysmorphic syndromes","volume":"36","author":"Al\u2010Gazali L","year":"1999","journal-title":"J Med Genet."}],"container-title":["Journal of Clinical Ultrasound"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.wiley.com\/onlinelibrary\/tdm\/v1\/articles\/10.1002%2Fjcu.20603","content-type":"unspecified","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/onlinelibrary.wiley.com\/doi\/pdf\/10.1002\/jcu.20603","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2023,11,14]],"date-time":"2023-11-14T13:47:02Z","timestamp":1699969622000},"score":1,"resource":{"primary":{"URL":"https:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/jcu.20603"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2009,5,27]]},"references-count":15,"journal-issue":{"issue":"7","published-print":{"date-parts":[[2009,9]]}},"alternative-id":["10.1002\/jcu.20603"],"URL":"https:\/\/doi.org\/10.1002\/jcu.20603","archive":["Portico"],"relation":{},"ISSN":["0091-2751","1097-0096"],"issn-type":[{"value":"0091-2751","type":"print"},{"value":"1097-0096","type":"electronic"}],"subject":[],"published":{"date-parts":[[2009,5,27]]}}}