{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,1,15]],"date-time":"2026-01-15T00:06:28Z","timestamp":1768435588076,"version":"3.49.0"},"reference-count":7,"publisher":"Ovid Technologies (Wolters Kluwer Health)","issue":"C","license":[{"start":{"date-parts":[[2021,1,1]],"date-time":"2021-01-01T00:00:00Z","timestamp":1609459200000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"},{"start":{"date-parts":[[2021,1,1]],"date-time":"2021-01-01T00:00:00Z","timestamp":1609459200000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/legal\/tdmrep-license"},{"start":{"date-parts":[[2021,1,18]],"date-time":"2021-01-18T00:00:00Z","timestamp":1610928000000},"content-version":"vor","delay-in-days":17,"URL":"http:\/\/creativecommons.org\/licenses\/by-nc-nd\/4.0\/"}],"content-domain":{"domain":["lww.com","ovid.com"],"crossmark-restriction":true},"short-container-title":[],"published-print":{"date-parts":[[2021,1]]},"abstract":"<jats:title>Abstract<\/jats:title>\n                  <jats:sec>\n                    <jats:title>Introduction<\/jats:title>\n                    <jats:p>Bartsocas-Papas syndrome (BPS) is an autosomal recessive form of Popliteal Pterygium syndrome (PPS). It is a very rare disease characterized by congenital craniofacial anomalies, popliteal webbing, and genitourinary and musculoskeletal anomalies. Almost all of the cases were reported in dead intrauterine pregnancies.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Presentation of case<\/jats:title>\n                    <jats:p>We present a 10-month-old boy with bilateral complete cleft lip and palate, abnormal scalp hair, an absence of both upper eyelids, choanal atresia, syndactyly of the third and fourth fingers of the right hand, agenesis fingers on the left hand, bilateral popliteal pterygia, bilateral talipes equinovarus, agenesis of the toes of both lower extremities, intercrural webbing, an absence of testis, and scrotal anomaly. Multistage surgical correction was performed for the multiple congenital malformations.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Conclusion<\/jats:title>\n                    <jats:p>We report the first case of BPS from Indonesia. Gradual management should be performed according to the patient's age and available facilities.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Highlights<\/jats:title>\n                  <\/jats:sec>","DOI":"10.1016\/j.ijscr.2021.01.070","type":"journal-article","created":{"date-parts":[[2021,1,27]],"date-time":"2021-01-27T07:55:55Z","timestamp":1611734155000},"page":"436-439","update-policy":"https:\/\/doi.org\/10.1097\/lww.0000000000001000","source":"Crossref","is-referenced-by-count":2,"title":["Bartsocas-Papas syndrome"],"prefix":"10.1097","volume":"79","author":[{"given":"Fonny","family":"Josh","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Tomie Hermawan","family":"Soekamto","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Djohansjah","family":"Marzoeki","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Muhammad","family":"Faruk","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"276","reference":[{"key":"R1-99-20260114","doi-asserted-by":"crossref","first-page":"222","DOI":"10.1136\/jmg.9.2.222","article-title":"Popliteal pterygium syndrome. Evidence for a severe autosomal recessive form","volume":"9","author":"Bartsocas","year":"1972","journal-title":"J. Med. Genet"},{"key":"R3-99-20260114","first-page":"1","article-title":"Bartsocas-Papas syndrome: unusual findings in the first reported egyptian family","volume":"2011","author":"Abdalla","year":"2011","journal-title":"Case Rep. Genet"},{"key":"R4-99-20260114","doi-asserted-by":"crossref","first-page":"226","DOI":"10.1016\/j.ijsu.2020.10.034","article-title":"The SCARE 2020 guideline: updating consensus surgical CAse REport (SCARE) guidelines","volume":"84","author":"Agha","year":"2020","journal-title":"Int. J. Surg"},{"key":"R5-99-20260114","doi-asserted-by":"crossref","first-page":"76","DOI":"10.1016\/j.ajhg.2011.11.014","article-title":"Mutations in RIPK4 cause the autosomal-recessive form of popliteal pterygium syndrome","volume":"90","author":"Kalay","year":"2012","journal-title":"Am. J. Hum. Genet"},{"key":"R6-99-20260114","doi-asserted-by":"crossref","first-page":"545","DOI":"10.1002\/ajmg.a.36896","article-title":"Expanding the genetic and phenotypic spectrum of popliteal pterygium disorders","volume":"167","author":"Leslie","year":"2015","journal-title":"Am. J. Med. Genet. Part A"},{"key":"R7-99-20260114","doi-asserted-by":"crossref","first-page":"31","DOI":"10.1186\/1755-8166-6-31","article-title":"De novo 2.3 Mb microdeletion of 1q32.2 involving the Van der Woude Syndrome locus","volume":"6","author":"Tan","year":"2013","journal-title":"Mol. Cytogenet"},{"key":"R9-99-20260114","doi-asserted-by":"crossref","first-page":"1434","DOI":"10.1097\/SCS.0000000000004698","article-title":"Van der Woude and Popliteal Pterygium Syndromes","volume":"29","author":"Bennun","year":"2018","journal-title":"J. Craniofac. Surg"}],"container-title":["International Journal of Surgery Case Reports"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S2210261221000729?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S2210261221000729?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/journals.lww.com\/10.1016\/j.ijscr.2021.01.070","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2026,1,14]],"date-time":"2026-01-14T13:33:27Z","timestamp":1768397607000},"score":1,"resource":{"primary":{"URL":"https:\/\/journals.lww.com\/10.1016\/j.ijscr.2021.01.070"}},"subtitle":["The first case report of severe autosomal recessive form from Indonesia"],"short-title":[],"issued":{"date-parts":[[2021,1]]},"references-count":7,"journal-issue":{"issue":"C","published-print":{"date-parts":[[2021]]}},"URL":"https:\/\/doi.org\/10.1016\/j.ijscr.2021.01.070","relation":{},"ISSN":["2210-2612"],"issn-type":[{"value":"2210-2612","type":"print"}],"subject":[],"published":{"date-parts":[[2021,1]]}}}