13(号染色体)三体型综合征文献(pubmed) 赞助商链接以下为句子列表:英文: 13 cases report of early diagnosis and treatment of fat embolism syndrome after bone fracture;中文: 骨折后脂肪栓塞综合征早期诊治13例报道 英文: MethodsThe concentrations of insulin in tears were measured by radioimmunodetection fro...
Trisomy 13, also known as Patau Syndrome, is a congenital malformation that leads to several ocular anomalies, of which cataracts are the most common, as well as iris and retinal colobomas, persistent hyperplastic primary vitreous, persistent tunica vasculosa lentis, and microphthalmos. While ...
A 61-year-old man was admitted to our hopital because of recurrent tonsillitis and anemia syndrome. On physical examination lymph node enlargement in both laterocervical and axillary areas was found. Peripheral blood count showed: hemoglobin 6.3 g/dL, hematocrit 20%, red blood cell count 1.88 ...
Periodontal disease in adolescent Down' syndrome patients. Clinical case presentation Behavior management was achieved with the 芦show-tell-do禄 technique alongside with voice control. Initial treatment consisted on sweeping brushing technique with parental assistance, use of dental floss (Dento Bacterial ...
Anatomical and histopathological findings in 12 cases of trisomy 13 syndrome (nine with classic full trisomy and three with trisomy 13 and an unbalanced Ro... P Moerman,JP Fryns,KVD Steen,... - 《Human Genetics》 被引量: 192发表: 1988年 Molecular approaches to the treatment, prophylaxis, ...
Ongoing assessment for and treatment of anxiety and other mood disorders should be continued through adolescence. Parents should be referred to support organizations, including Klinefelter Syndrome and Associates (www.genetic.org) and Triplo-X Syndrome (www.triplo-X.org). Show moreView chapter Chapter...
13,14. Recently, a case of Down syndrome was genetically identified in Neolithic Ireland (3629–3371 BCE), although no physical description was given15. However, we are aware of no prehistoric or historic cases of either trisomy 13 or 18 that have been identified genetically or osteologically....
A clinically similar hemophagocytic CSS in autoinflammatory and autoimmune disorders is called macrophage activation syndrome (MAS) [6–8]. Iatrogenic CSS, including cytokine release syndromes after immunotherapy (e.g., OKT3 infusions), and chimeric antigen receptor (CAR) T-cell treatment are ...
The 50th anniversary of the discovery of trisomy 21: The past, present, and future of research and treatment of Down syndrome Trisomy 21 or Down syndrome is a chromosomal disorder resulting from the presence of all or part of an extra Chromosome 21. It is a common birth defect, th... M...
Examination of a first-trimester Down syndrome screening concept on a mix of 11,107 high- and low-risk patients at a private center for prenatal medicine i... To assess the performance of a combined first-trimester screening concept for trisomies 21, 18 and 13 applied to a low- and high...