lutein 发表于 2025-3-21 20:04:45
书目名称Congenital Adrenal Hyperplasia影响因子(影响力)<br> http://impactfactor.cn/if/?ISSN=BK0235468<br><br> <br><br>书目名称Congenital Adrenal Hyperplasia影响因子(影响力)学科排名<br> http://impactfactor.cn/ifr/?ISSN=BK0235468<br><br> <br><br>书目名称Congenital Adrenal Hyperplasia网络公开度<br> http://impactfactor.cn/at/?ISSN=BK0235468<br><br> <br><br>书目名称Congenital Adrenal Hyperplasia网络公开度学科排名<br> http://impactfactor.cn/atr/?ISSN=BK0235468<br><br> <br><br>书目名称Congenital Adrenal Hyperplasia被引频次<br> http://impactfactor.cn/tc/?ISSN=BK0235468<br><br> <br><br>书目名称Congenital Adrenal Hyperplasia被引频次学科排名<br> http://impactfactor.cn/tcr/?ISSN=BK0235468<br><br> <br><br>书目名称Congenital Adrenal Hyperplasia年度引用<br> http://impactfactor.cn/ii/?ISSN=BK0235468<br><br> <br><br>书目名称Congenital Adrenal Hyperplasia年度引用学科排名<br> http://impactfactor.cn/iir/?ISSN=BK0235468<br><br> <br><br>书目名称Congenital Adrenal Hyperplasia读者反馈<br> http://impactfactor.cn/5y/?ISSN=BK0235468<br><br> <br><br>书目名称Congenital Adrenal Hyperplasia读者反馈学科排名<br> http://impactfactor.cn/5yr/?ISSN=BK0235468<br><br> <br><br>轻弹 发表于 2025-3-21 20:38:09
Recent Advances: The Fasciculata and Glomerulosa as Two Distinct Glands, (1970) suggested that an 11 .-hydroxylase defect might occur only in the fasciculata, sparing the glomerulosa from an 11 .-hydroxylase deficiency. The hypothesis accounts for the rise in aldosterone secretion observed in a patient with 11 .-hydroxylase deficiency after excessive DOC levels were supCarcinogen 发表于 2025-3-22 02:38:54
Treatment,he efficacy of cortisone therapy for CAH due to 21-hydroxylase deficiency (Wilkins et al. 1950; Bartter et al. 1951; Bartter 1977), glucocorticoid therapy has been the keystone of treatment for this disorder. Glucocorticoid administration both replaces the deficient Cortisol and suppresses ACTH over具体 发表于 2025-3-22 08:20:18
Pubertal Development,nological age (John and Verkauf 1971; Ghali et al. 1977; Klingensmith et al. 1977; Pang et al. 1977 a). The pattern of gonadotropin response to LH-RH is appropriate for age in well-controlled prepubertal and pubertal female patients (Kirkland et al. 1974; Reiter et al. 1975). These normal findings sCubicle 发表于 2025-3-22 11:47:25
Genetics,traits (Childs et al. 1956; Prader 1958; Wilkins 1962). Males and females are equally at risk (Baulieu et al. 1967). Although there are exceptions (Rosen- bloom and Smith 1966), the clinical presentation—simple virilizing or salt-wasting—is usually consistent within one family. In Europe and the USAjagged 发表于 2025-3-22 13:24:50
Prenatal Diagnosis,niotic fluid of the affected fetus, several investigators have attempted the prenatal diagnosis by measurement of various hormones (New and Levine 1973). Most recently, elevated levels of 17-OHP (Frasier et al. 1975; Nagamani et al. 1978; Hughes and Laurence 1979; Pang et al. 1980b) and Δ. (Pang etjagged 发表于 2025-3-22 17:34:27
http://reply.papertrans.cn/24/2355/235468/235468_7.png莎草 发表于 2025-3-22 22:30:55
,Electron–Specimen Interactions., suppressed by treatment, natriuresis occurs and renin-angiotensin levels consequently rise, stimulating the glomerulosa to synthesize aldosterone (Fig. 9). Because the glomerulosa, unlike the fasciculata, is spared the 11 .-hydroxylase defect, it can respond to this stimulation with an appropriatefebrile 发表于 2025-3-23 04:03:45
http://reply.papertrans.cn/24/2355/235468/235468_9.png条街道往前推 发表于 2025-3-23 07:13:43
,Electron–Specimen Interactions.,t 50—80% of patients with 21-hydroxylase deficiency (Cohen 1969; Rimoin and Schimke 1971; Fife and Rappaport 1983). A very high incidence of salt-wasting CAH has been found among the Yupiks (Hirschfeld and Fleshman 1969).