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Initial Presentation of Haemophilia B in a 3-month-old Infant - A Case Report and Literature Review 1例3月龄婴儿首次出现B型血友病- 1例报告及文献复习
MedPress Pediatrics and Child Health Care Pub Date : 2022-08-30 DOI: 10.33582/mppchc.2022.202207002
Huda Ali Mohamed, N. Ghazy, Heba AlAmiri, Hasa AlNuaimi, Aysha Al-Kaabi, Haydar J. AlRufaye
{"title":"Initial Presentation of Haemophilia B in a 3-month-old Infant - A Case Report and Literature Review","authors":"Huda Ali Mohamed, N. Ghazy, Heba AlAmiri, Hasa AlNuaimi, Aysha Al-Kaabi, Haydar J. AlRufaye","doi":"10.33582/mppchc.2022.202207002","DOIUrl":"https://doi.org/10.33582/mppchc.2022.202207002","url":null,"abstract":"Hemophilia B, also known as Christmas disease, is an X-linked disorder caused by either the absence or reduced biosynthesis of clotting factor IX.","PeriodicalId":214880,"journal":{"name":"MedPress Pediatrics and Child Health Care","volume":"21 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2022-08-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"124001155","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Gaucher Disease in a 15-month-Old Child: A Case Report and Literature Review 15月龄儿童戈谢病1例报告并文献复习
MedPress Pediatrics and Child Health Care Pub Date : 2022-08-22 DOI: 10.33582/mppchc.2022.202207001
S. Hamwi, Huda Ali Mohamed, Abdulqader Jalani Al Zubaidi, Alaa Sattar Mehair, Amar Al Shibli
{"title":"Gaucher Disease in a 15-month-Old Child: A Case Report and Literature Review","authors":"S. Hamwi, Huda Ali Mohamed, Abdulqader Jalani Al Zubaidi, Alaa Sattar Mehair, Amar Al Shibli","doi":"10.33582/mppchc.2022.202207001","DOIUrl":"https://doi.org/10.33582/mppchc.2022.202207001","url":null,"abstract":"Gaucher Disease (GD) is an autosomal recessive systemic lysosomal storage disorder, characterized by glucocerebroside deposition in cells of macrophage-monocyte system and accumulation of glucosylceramide in different organs as result of deficiency in lysosomal β-glycosidase (glucocerebrosidase).","PeriodicalId":214880,"journal":{"name":"MedPress Pediatrics and Child Health Care","volume":"10 1 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2022-08-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"125821703","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
The Potential Benefit of Improving Health Literacy to Reduce Socioeconomic Inequities in Adolescent Health and Educational Outcomes. 提高健康素养以减少青少年健康和教育成果方面的社会经济不平等的潜在益处。
MedPress Pediatrics and Child Health Care Pub Date : 2022-05-06 DOI: 10.33582/mppchc.2022.202203003
Shuaijun Guo, Xiao-ming Yu, Fan He, E. Davis, R. Armstrong, L. Naccarella
{"title":"The Potential Benefit of Improving Health Literacy to Reduce Socioeconomic Inequities in Adolescent Health and Educational Outcomes.","authors":"Shuaijun Guo, Xiao-ming Yu, Fan He, E. Davis, R. Armstrong, L. Naccarella","doi":"10.33582/mppchc.2022.202203003","DOIUrl":"https://doi.org/10.33582/mppchc.2022.202203003","url":null,"abstract":"Background: Exposure to early socioeconomic disadvantage is associated with a range of adverse health and educational outcomes in later life, leading to substantial social and economic costs.","PeriodicalId":214880,"journal":{"name":"MedPress Pediatrics and Child Health Care","volume":"115 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2022-05-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"133598705","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Retinopathy of Prematurity and Risk Factors 早产儿视网膜病变及其危险因素
MedPress Pediatrics and Child Health Care Pub Date : 2022-05-06 DOI: 10.33582/mppchc.2022.202203001
Rawia Eltahir, S. Javed, Nyaish Mansoor, T. Mansoor, Kirandeep Bhavra, Timothy K Reynolds, Mansoor Ahmed
{"title":"Retinopathy of Prematurity and Risk Factors","authors":"Rawia Eltahir, S. Javed, Nyaish Mansoor, T. Mansoor, Kirandeep Bhavra, Timothy K Reynolds, Mansoor Ahmed","doi":"10.33582/mppchc.2022.202203001","DOIUrl":"https://doi.org/10.33582/mppchc.2022.202203001","url":null,"abstract":"Background: Retinopathy of Prematurity (ROP) is a condition confined to the premature retina. Hence, it is more commonly associated with extreme prematurity and low birth weight.","PeriodicalId":214880,"journal":{"name":"MedPress Pediatrics and Child Health Care","volume":"2 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2022-05-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"132382009","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
A Case of Familial Complete Androgen Insensitivity Syndrome- Baby with Three Mothers and the Daughter shows the Mother - Challenges and Threats in Advanced Assisted Reproduction Technology 家族性完全雄激素不敏感综合征一例——三母三女——先进辅助生殖技术的挑战与威胁
MedPress Pediatrics and Child Health Care Pub Date : 2022-05-06 DOI: 10.33582/mppchc.2022.202203002
Neeva D. Govani, Dhaval R. Govani, Namrata G. Panchasara, Rasila R. Patel, Partap Kumar Midha, Ramnik V. Patel
{"title":"A Case of Familial Complete Androgen Insensitivity Syndrome- Baby with Three Mothers and the Daughter shows the Mother - Challenges and Threats in Advanced Assisted Reproduction Technology","authors":"Neeva D. Govani, Dhaval R. Govani, Namrata G. Panchasara, Rasila R. Patel, Partap Kumar Midha, Ramnik V. Patel","doi":"10.33582/mppchc.2022.202203002","DOIUrl":"https://doi.org/10.33582/mppchc.2022.202203002","url":null,"abstract":"We wish to present a very unusual case of an inheritance of a very rare disease, familial complete androgen insensitivity syndrome, in a baby girl with three mothers and the mother being a known case of complete androgen insensitive syndrome.","PeriodicalId":214880,"journal":{"name":"MedPress Pediatrics and Child Health Care","volume":"69 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2022-05-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"123889248","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
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