一个罕见的家庭患有辛普森-戈拉比-贝梅尔综合征与罕见的表现在母亲和两个儿子

Q4 Medicine

Pediatria Polska Pub Date : 2023-01-01 DOI:10.5114/polp.2023.131546

Kamil Możdżeń, Agnieszka Murawska, Julia Hypnar, Edward Pędziwiatr, Jakub Pośpiech, Kinga Kowalska-Duplaga

{"title":"一个罕见的家庭患有辛普森-戈拉比-贝梅尔综合征与罕见的表现在母亲和两个儿子","authors":"Kamil Możdżeń, Agnieszka Murawska, Julia Hypnar, Edward Pędziwiatr, Jakub Pośpiech, Kinga Kowalska-Duplaga","doi":"10.5114/polp.2023.131546","DOIUrl":null,"url":null,"abstract":"AMA Możdżeń K, Murawska A, Hypnar J, Pędziwiatr E, Pośpiech J, Kowalska-Duplaga K. A rare case of family suffering from Simpson-Golabi-Behmel syndrome with an uncommon manifestation in a mother and 2 sons. Pediatria Polska - Polish Journal of Paediatrics. 2023. doi:10.5114/polp.2023.131546. APA Możdżeń, K., Murawska, A., Hypnar, J., Pędziwiatr, E., Pośpiech, J., & Kowalska-Duplaga, K. (2023). A rare case of family suffering from Simpson-Golabi-Behmel syndrome with an uncommon manifestation in a mother and 2 sons. Pediatria Polska - Polish Journal of Paediatrics. https://doi.org/10.5114/polp.2023.131546 Chicago Możdżeń, Kamil, Agnieszka Murawska, Julia Hypnar, Edward Pędziwiatr, Jakub Pośpiech, and Kinga Kowalska-Duplaga. 2023. \"A rare case of family suffering from Simpson-Golabi-Behmel syndrome with an uncommon manifestation in a mother and 2 sons\". Pediatria Polska - Polish Journal of Paediatrics. doi:10.5114/polp.2023.131546. Harvard Możdżeń, K., Murawska, A., Hypnar, J., Pędziwiatr, E., Pośpiech, J., and Kowalska-Duplaga, K. (2023). A rare case of family suffering from Simpson-Golabi-Behmel syndrome with an uncommon manifestation in a mother and 2 sons. Pediatria Polska - Polish Journal of Paediatrics. https://doi.org/10.5114/polp.2023.131546 MLA Możdżeń, Kamil et al. \"A rare case of family suffering from Simpson-Golabi-Behmel syndrome with an uncommon manifestation in a mother and 2 sons.\" Pediatria Polska - Polish Journal of Paediatrics, 2023. doi:10.5114/polp.2023.131546. Vancouver Możdżeń K, Murawska A, Hypnar J, Pędziwiatr E, Pośpiech J, Kowalska-Duplaga K. A rare case of family suffering from Simpson-Golabi-Behmel syndrome with an uncommon manifestation in a mother and 2 sons. Pediatria Polska - Polish Journal of Paediatrics. 2023. doi:10.5114/polp.2023.131546.","PeriodicalId":39653,"journal":{"name":"Pediatria Polska","volume":"45 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"A rare case of family suffering from Simpson-Golabi-Behmel syndrome with an uncommon manifestation in a mother and 2 sons\",\"authors\":\"Kamil Możdżeń, Agnieszka Murawska, Julia Hypnar, Edward Pędziwiatr, Jakub Pośpiech, Kinga Kowalska-Duplaga\",\"doi\":\"10.5114/polp.2023.131546\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"AMA Możdżeń K, Murawska A, Hypnar J, Pędziwiatr E, Pośpiech J, Kowalska-Duplaga K. A rare case of family suffering from Simpson-Golabi-Behmel syndrome with an uncommon manifestation in a mother and 2 sons. Pediatria Polska - Polish Journal of Paediatrics. 2023. doi:10.5114/polp.2023.131546. APA Możdżeń, K., Murawska, A., Hypnar, J., Pędziwiatr, E., Pośpiech, J., & Kowalska-Duplaga, K. (2023). A rare case of family suffering from Simpson-Golabi-Behmel syndrome with an uncommon manifestation in a mother and 2 sons. Pediatria Polska - Polish Journal of Paediatrics. https://doi.org/10.5114/polp.2023.131546 Chicago Możdżeń, Kamil, Agnieszka Murawska, Julia Hypnar, Edward Pędziwiatr, Jakub Pośpiech, and Kinga Kowalska-Duplaga. 2023. \\\"A rare case of family suffering from Simpson-Golabi-Behmel syndrome with an uncommon manifestation in a mother and 2 sons\\\". Pediatria Polska - Polish Journal of Paediatrics. doi:10.5114/polp.2023.131546. Harvard Możdżeń, K., Murawska, A., Hypnar, J., Pędziwiatr, E., Pośpiech, J., and Kowalska-Duplaga, K. (2023). A rare case of family suffering from Simpson-Golabi-Behmel syndrome with an uncommon manifestation in a mother and 2 sons. Pediatria Polska - Polish Journal of Paediatrics. https://doi.org/10.5114/polp.2023.131546 MLA Możdżeń, Kamil et al. \\\"A rare case of family suffering from Simpson-Golabi-Behmel syndrome with an uncommon manifestation in a mother and 2 sons.\\\" Pediatria Polska - Polish Journal of Paediatrics, 2023. doi:10.5114/polp.2023.131546. Vancouver Możdżeń K, Murawska A, Hypnar J, Pędziwiatr E, Pośpiech J, Kowalska-Duplaga K. A rare case of family suffering from Simpson-Golabi-Behmel syndrome with an uncommon manifestation in a mother and 2 sons. Pediatria Polska - Polish Journal of Paediatrics. 2023. doi:10.5114/polp.2023.131546.\",\"PeriodicalId\":39653,\"journal\":{\"name\":\"Pediatria Polska\",\"volume\":\"45 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2023-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Pediatria Polska\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.5114/polp.2023.131546\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"Medicine\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Pediatria Polska","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.5114/polp.2023.131546","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"Medicine","Score":null,"Total":0}

引用次数: 0

摘要

AMA Możdżeń K、Murawska A、Hypnar J、Pędziwiatr E、Pośpiech J、Kowalska-Duplaga K.一例罕见的辛普森-戈拉比-贝梅尔综合征家庭病例，母亲和两个儿子都有不常见的表现。Pediatria Polska - Polish Journal of Paediatrics.2023. doi:10.5114/polp.2023.131546.APA Możdżeń, K., Murawska, A., Hypnar, J., Pędziwiatr, E., Pośpiech, J., & Kowalska-Duplaga, K. (2023)。一个罕见的辛普森-戈拉比-贝梅尔综合征家庭病例，母亲和两个儿子都有不常见的表现。https://doi.org/10.5114/polp.2023.131546 Chicago Możdżeń, Kamil, Agnieszka Murawska, Julia Hypnar, Edward Pędziwiatr, Jakub Pośpiech, and Kinga Kowalska-Duplaga.2023."罕见的 Simpson-Golabi-Behmel 综合征家庭病例，母亲和两个儿子的罕见表现》。doi:10.5114/polp.2023.131546。Harvard Możdżeń, K., Murawska, A., Hypnar, J., Pędziwiatr, E., Pośpiech, J., and Kowalska-Duplaga, K. (2023).一个罕见的辛普森-戈拉比-贝梅尔综合征家庭病例，母亲和两个儿子都有不常见的表现。https://doi.org/10.5114/polp.2023.131546 MLA Możdżeń, Kamil et al. "A rare case of family suffering from Simpson-Golabi-Behmel syndrome with an uncommon manifestation in a mother and 2 sons." Pediatria Polska - Polish Journal of Paediatrics.doi:10.5114/polp.2023.131546.Vancouver Możdżeń K, Murawska A, Hypnar J, Pędziwiatr E, Pośpiech J, Kowalska-Duplaga K. A rare case of family suffering from Simpson-Golabi-Behmel syndrome with an uncommon manifestation in a mother and two sons.Pediatria Polska - Polish Journal of Paediatrics.2023. doi:10.5114/polp.2023.131546.

本文章由计算机程序翻译，如有差异，请以英文原文为准。

查看原文本刊更多论文

A rare case of family suffering from Simpson-Golabi-Behmel syndrome with an uncommon manifestation in a mother and 2 sons

AMA Możdżeń K, Murawska A, Hypnar J, Pędziwiatr E, Pośpiech J, Kowalska-Duplaga K. A rare case of family suffering from Simpson-Golabi-Behmel syndrome with an uncommon manifestation in a mother and 2 sons. Pediatria Polska - Polish Journal of Paediatrics. 2023. doi:10.5114/polp.2023.131546. APA Możdżeń, K., Murawska, A., Hypnar, J., Pędziwiatr, E., Pośpiech, J., & Kowalska-Duplaga, K. (2023). A rare case of family suffering from Simpson-Golabi-Behmel syndrome with an uncommon manifestation in a mother and 2 sons. Pediatria Polska - Polish Journal of Paediatrics. https://doi.org/10.5114/polp.2023.131546 Chicago Możdżeń, Kamil, Agnieszka Murawska, Julia Hypnar, Edward Pędziwiatr, Jakub Pośpiech, and Kinga Kowalska-Duplaga. 2023. "A rare case of family suffering from Simpson-Golabi-Behmel syndrome with an uncommon manifestation in a mother and 2 sons". Pediatria Polska - Polish Journal of Paediatrics. doi:10.5114/polp.2023.131546. Harvard Możdżeń, K., Murawska, A., Hypnar, J., Pędziwiatr, E., Pośpiech, J., and Kowalska-Duplaga, K. (2023). A rare case of family suffering from Simpson-Golabi-Behmel syndrome with an uncommon manifestation in a mother and 2 sons. Pediatria Polska - Polish Journal of Paediatrics. https://doi.org/10.5114/polp.2023.131546 MLA Możdżeń, Kamil et al. "A rare case of family suffering from Simpson-Golabi-Behmel syndrome with an uncommon manifestation in a mother and 2 sons." Pediatria Polska - Polish Journal of Paediatrics, 2023. doi:10.5114/polp.2023.131546. Vancouver Możdżeń K, Murawska A, Hypnar J, Pędziwiatr E, Pośpiech J, Kowalska-Duplaga K. A rare case of family suffering from Simpson-Golabi-Behmel syndrome with an uncommon manifestation in a mother and 2 sons. Pediatria Polska - Polish Journal of Paediatrics. 2023. doi:10.5114/polp.2023.131546.

求助全文

通过发布文献求助，成功后即可免费获取论文全文。去求助

来源期刊

Pediatria Polska Medicine-Pediatrics, Perinatology and Child Health

CiteScore

0.40

自引率

0.00%

发文量

期刊介绍： Pediatria Polska - rzetelna wiedza i tradycja. Organ Polskiego Towarzystwa Pediatrycznego. Ukazuje się od 1921 roku, poprzednio w latach 1908-1920 jako Przegląd Pedyatryczny. Drugie obok Otolaryngologii Polskiej najstarsze czasopismo medyczne ukazujące się na polskim rynku. Czasopismo zamieszcza doświadczalne i kliniczne prace oryginalne oraz opisy rzadko występujących i trudnych diagnostycznie przypadków klinicznych. W Pediatrii Polskiej publikowane są także obszerne omówienia poglądowe problemów pediatrycznych oparte na najnowszym piśmiennictwie światowym.