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International Journal of Pediatric Health Care & Advancements最新文献

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Spectacular Presentation of Tuberous Xanthomas in a Case of Familial Hypercholesterolemia Type IIa 家族性高胆固醇血症IIa型的结节性黄斑瘤的惊人表现
International Journal of Pediatric Health Care & Advancements Pub Date : 2018-11-28 DOI: 10.19070/2572-7354-1800025
Morocco.
{"title":"Spectacular Presentation of Tuberous Xanthomas in a Case of Familial Hypercholesterolemia Type IIa","authors":"Morocco.","doi":"10.19070/2572-7354-1800025","DOIUrl":"https://doi.org/10.19070/2572-7354-1800025","url":null,"abstract":"Xanthomas are benign lesions that may manifest as papules or nodules in skin, characterized by the accumulation of lipids on macrophages that develop in the subcutaneous tissue [1]. Tuberous xanthomas are yellow or red, firms nodules, most commonly seen on the extensor members of the limbs and buttocks [2]. They are observed in several lipidoses and generally indicate a trouble of lipoprotein metabolism, in particular familial hypercholesterolemia, and generally do not exceed 2 cm [3].","PeriodicalId":240593,"journal":{"name":"International Journal of Pediatric Health Care & Advancements","volume":"25 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2018-11-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"125993136","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
Acute Generalized Exanthematous Pustulosis in a Child without Drug Intake: Clinical and Histological Features 无药物摄入的儿童急性全身性发疹性脓疱病:临床和组织学特征
International Journal of Pediatric Health Care & Advancements Pub Date : 2018-11-28 DOI: 10.19070/2572-7354-1800027
G. Senhaji, Mernissi Fz
{"title":"Acute Generalized Exanthematous Pustulosis in a Child without Drug Intake: Clinical and Histological Features","authors":"G. Senhaji, Mernissi Fz","doi":"10.19070/2572-7354-1800027","DOIUrl":"https://doi.org/10.19070/2572-7354-1800027","url":null,"abstract":"","PeriodicalId":240593,"journal":{"name":"International Journal of Pediatric Health Care & Advancements","volume":"3 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2018-11-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"115884450","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 Management of Hereditary Epidermolysis Bullosa: Experience of a Moroccan Sub-Population 遗传性大疱性表皮松解症的治疗:摩洛哥亚群的经验
International Journal of Pediatric Health Care & Advancements Pub Date : 2018-09-26 DOI: 10.19070/2572-7354-1800024
Y Barbach, Mernissi Fz
{"title":"The Management of Hereditary Epidermolysis Bullosa: Experience of a Moroccan Sub-Population","authors":"Y Barbach, Mernissi Fz","doi":"10.19070/2572-7354-1800024","DOIUrl":"https://doi.org/10.19070/2572-7354-1800024","url":null,"abstract":"Hereditary epidermolysis bullosa (HEB) is rare genodermatose characterized by epithelial fragility leading to the formation of bubbles, cutaneous and mucosal erosions [1]. They would affect about 1/50000 to 1/20000 newborns [2]. The cause of this genodermatosis is a deficiency of one of the proteins involved in anchoring the epidermis to the dermis. The deficient protein determines the level of bubble formation and, therefore, the form and severity of the EB subtype. This is a basis for classification. The resulting form is the result of an autoimmune reaction against collagen VII, the protein anchoring fibrils in the papillary dermis, causing detachment of the epidermis. The clinical severity is variable, ranging from minor functional discomfort to the death of the child, to the culprits responsible for severe disabilities, to the infectious, nutritional, cicatricial and functional complications they cause. The aim of this work is to describe the particularities of HEB in our population epidemiologically, clinically, as well as the search for different complications in order to establish a good therapeutic management.","PeriodicalId":240593,"journal":{"name":"International Journal of Pediatric Health Care & Advancements","volume":"182 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2018-09-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"115565201","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
Isolated Genital Psoriasis 孤立性生殖器牛皮癣
International Journal of Pediatric Health Care & Advancements Pub Date : 2018-09-26 DOI: 10.19070/2572-7354-1800023
O. ElJouari, Zaougui Aa
{"title":"Isolated Genital Psoriasis","authors":"O. ElJouari, Zaougui Aa","doi":"10.19070/2572-7354-1800023","DOIUrl":"https://doi.org/10.19070/2572-7354-1800023","url":null,"abstract":"Isolated genital psoriasis is a variety of autoimmune dermatological disease, which can have an onset in all age groups. It is considered a rare manifestation of psoriasis. It is most often diagnosed at an advanced stage [1]. The manifestations of genital psoriasis may differ from typical genital dermatoses and may mimic other diseases at an early stage. Relapsing-remitting course of psoriasis is another factor limiting adequate diagnosis [2]. The objective of this article is to report a case of an isolated genital psoriasis and to review the literature, emphasizing the underdiagnosis of this condition.","PeriodicalId":240593,"journal":{"name":"International Journal of Pediatric Health Care & Advancements","volume":"58 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2018-09-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"114986742","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: 1
Trichotillomania of Eyelashes: An Uncommon Disorder 睫毛拔毛癖:一种罕见的疾病
International Journal of Pediatric Health Care & Advancements Pub Date : 2018-07-23 DOI: 10.19070/2572-7354-1800022
O. ElJouari, Zaougui Aa
{"title":"Trichotillomania of Eyelashes: An Uncommon Disorder","authors":"O. ElJouari, Zaougui Aa","doi":"10.19070/2572-7354-1800022","DOIUrl":"https://doi.org/10.19070/2572-7354-1800022","url":null,"abstract":"","PeriodicalId":240593,"journal":{"name":"International Journal of Pediatric Health Care & Advancements","volume":"1 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2018-07-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"125865925","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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