{"title":"双侧腓骨瓣裂伴镜足1例","authors":"E. Abdalla, Israa Alaa-Eddin","doi":"10.4172/2157-7412.1000I102","DOIUrl":null,"url":null,"abstract":"Volume 7 • Issue 2 • 1000i102 J Genet Syndr Gene Ther ISSN: 2157-7412 JGSGT, an open access journal A two-month-old male infant presented with peculiar bilateral lower limb malformations. He was born at term to unrelated healthy Egyptian parents after an uncomplicated pregnancy and delivery. There was no history of drug use, alcohol intake or exposure to teratogenic agents in pregnancy and the family history was also unremarkable.","PeriodicalId":89584,"journal":{"name":"Journal of genetic syndromes & gene therapy","volume":"59 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2016-02-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":"{\"title\":\"Bilateral Fibular Dimelia with Mirror Foot: An Additional Case Report\",\"authors\":\"E. Abdalla, Israa Alaa-Eddin\",\"doi\":\"10.4172/2157-7412.1000I102\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Volume 7 • Issue 2 • 1000i102 J Genet Syndr Gene Ther ISSN: 2157-7412 JGSGT, an open access journal A two-month-old male infant presented with peculiar bilateral lower limb malformations. He was born at term to unrelated healthy Egyptian parents after an uncomplicated pregnancy and delivery. There was no history of drug use, alcohol intake or exposure to teratogenic agents in pregnancy and the family history was also unremarkable.\",\"PeriodicalId\":89584,\"journal\":{\"name\":\"Journal of genetic syndromes & gene therapy\",\"volume\":\"59 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2016-02-12\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"1\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of genetic syndromes & gene therapy\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.4172/2157-7412.1000I102\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of genetic syndromes & gene therapy","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.4172/2157-7412.1000I102","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Bilateral Fibular Dimelia with Mirror Foot: An Additional Case Report
Volume 7 • Issue 2 • 1000i102 J Genet Syndr Gene Ther ISSN: 2157-7412 JGSGT, an open access journal A two-month-old male infant presented with peculiar bilateral lower limb malformations. He was born at term to unrelated healthy Egyptian parents after an uncomplicated pregnancy and delivery. There was no history of drug use, alcohol intake or exposure to teratogenic agents in pregnancy and the family history was also unremarkable.
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