{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,7,4]],"date-time":"2025-07-04T22:05:51Z","timestamp":1751666751224},"reference-count":7,"publisher":"Springer Science and Business Media LLC","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2023,10,1]]},"DOI":"10.7759\/cureus.46328","type":"journal-article","created":{"date-parts":[[2023,10,1]],"date-time":"2023-10-01T20:01:20Z","timestamp":1696190480000},"source":"Crossref","is-referenced-by-count":1,"title":["Ambiguous Genitalia: An Unexpected Diagnosis in a Newborn"],"prefix":"10.7759","author":[{"given":"Ana","family":"Losa","sequence":"first","affiliation":[]},{"given":"Juliana","family":"Da Silva Cardoso","sequence":"additional","affiliation":[]},{"given":"Sara","family":"Leite","sequence":"additional","affiliation":[]},{"given":"Ana Cristina","family":"Barros","sequence":"additional","affiliation":[]},{"given":"Ana","family":"Guedes","sequence":"additional","affiliation":[]},{"given":"Cidade","family":"Rodrigues","sequence":"additional","affiliation":[]},{"given":"Teresa","family":"Borges","sequence":"additional","affiliation":[]},{"given":"Nat\u00e1lia","family":"Oliva-Teles","sequence":"additional","affiliation":[]},{"given":"Ana Rita","family":"Soares","sequence":"additional","affiliation":[]},{"given":"C\u00e9u","family":"Mota","sequence":"additional","affiliation":[]}],"member":"297","reference":[{"key":"ref1","doi-asserted-by":"publisher","DOI":"10.1016\/S2213-8587(18)30339-5","article-title":"A clinical algorithm to diagnose differences of sex development","volume":"7","author":"Le\u00f3n NY","year":"2019","unstructured":"Le\u00f3n NY, Reyes AP, Harley VR. A clinical algorithm to diagnose differences of sex development. Lancet Diabetes Endocrinol. 2019, 7:560-74. 10.1016\/S2213-8587(18)30339-5","journal-title":"Lancet Diabetes Endocrinol"},{"key":"ref2","doi-asserted-by":"publisher","DOI":"10.1038\/s41574-018-0010-8","article-title":"Caring for individuals with a difference of sex development (DSD): a consensus statement","volume":"14","author":"Cools M","year":"2018","unstructured":"Cools M, Nordenstr\u00f6m A, Robeva R, et al.. Caring for individuals with a difference of sex development (DSD): a consensus statement. Nat Rev Endocrinol. 2018, 14:415-29. 10.1038\/s41574-018-0010-8","journal-title":"Nat Rev Endocrinol"},{"key":"ref3","doi-asserted-by":"publisher","DOI":"10.1155\/2016\/5467083","article-title":"Cri-du-chat syndrome: clinical profile and chromosomal microarray analysis in six patients","volume":"2016","author":"Espirito Santo LD","year":"2016","unstructured":"Espirito Santo LD, Moreira LM, Riegel M. Cri-du-chat syndrome: clinical profile and chromosomal microarray analysis in six patients. Biomed Res Int. 2016, 2016:5467083. 10.1155\/2016\/5467083","journal-title":"Biomed Res Int"},{"key":"ref4","article-title":"Cri-du-chat syndrome","author":"Ajitkumar A","year":"2022","unstructured":"Ajitkumar A, Jamil RT, Mathai JK. Cri-du-chat syndrome. StatPearls. StatPearls Publishing, Treasure Island (FL); 2022."},{"key":"ref5","doi-asserted-by":"crossref","DOI":"10.1017\/S0012162201002419","article-title":"Cri du chat syndrome: genotype-phenotype correlations and recommendations for clinical management","volume":"44","author":"Cornish K","year":"2002","unstructured":"Cornish K, Bramble D. Cri du chat syndrome: genotype-phenotype correlations and recommendations for clinical management. Dev Med Child Neurol. 2002, 44:494-7.","journal-title":"Dev Med Child Neurol"},{"key":"ref6","doi-asserted-by":"publisher","DOI":"10.4081\/pr.2019.7839","article-title":"Children and adults affected by Cri du Chat syndrome: Care\u2019s recommendations","volume":"11","author":"Liverani ME","year":"2019","unstructured":"Liverani ME, Spano A, Danesino C, Malacarne M, Cavani S, Spunton M, Guala A. Children and adults affected by Cri du Chat syndrome: Care\u2019s recommendations. Pediatr Rep. 2019, 11:7839. 10.4081\/pr.2019.7839","journal-title":"Pediatr Rep"},{"key":"ref7","unstructured":"Duplications of 3q. (2008). Accessed. September 30, 2023: https:\/\/www.rarechromo.org\/media\/information\/Chromosome%20%203\/3q%20duplications%20FTNW.pdf."}],"container-title":["Cureus"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/www.cureus.com\/articles\/189723-ambiguous-genitalia-an-unexpected-diagnosis-in-a-newborn","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2024,2,9]],"date-time":"2024-02-09T20:09:59Z","timestamp":1707509399000},"score":1,"resource":{"primary":{"URL":"https:\/\/www.cureus.com\/articles\/189723-ambiguous-genitalia-an-unexpected-diagnosis-in-a-newborn"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2023,10,1]]},"references-count":7,"URL":"https:\/\/doi.org\/10.7759\/cureus.46328","relation":{},"ISSN":["2168-8184"],"issn-type":[{"value":"2168-8184","type":"print"}],"subject":[],"published":{"date-parts":[[2023,10,1]]}}}