adrenogenital syndrome
Adrenal Cortical Adenoma Arising in a Girl with Congenital Adrenogenital Syndrome
... Adrenal Cortical Adenoma Arising in a Girl with Congenital Adrenogenital Syndrome. http://pediatrics.aappublications.org/content/36/1/140[r] ...
5
ADRENOGENITAL SYNDROME IN A MALE CHILD DUE TO ADRENOCORTICAL TUMOR
... The purpose of this paper is to report the case of a boy with adrenogenital syndrome due to adrenocortical tumor with the unusual association of hemihypertrophy and the subsequent develo[r] ...
11
TRIAMCINOLONE THERAPY IN THE ADRENOGENITAL SYNDROME
... margin of safety, and cortisone, hydro- cortisone, or prednisone remain the drugs of choice in treatment of congenital vinilizing adrenal hyperplasia. Addendum[r] ...
10
In Vitro Hydroxylation of Steroids by Whole Adrenal Homogenates of Beef, Normal Man, and Patients with the Adrenogenital Syndrome
... This study gives direct evidence of a deficiency of 21-hydroxylation: Two diseased adrenal glands were unable to convert 17-hydroxyprogesterone into either 11-desoxycortisol or cortisol;[r] ...
7
THE ADRENOGENITAL SYNDROME, SALT-LOSING TYPE
... of cortisone during the interval was low and the urinary output of 17-ketosteroids increased to high levels. and the scrotum corrugated and dark brown (Fig[r] ...
17
THE EFFECTS OF ADRENOCORTICOTROPIC HORMONE AND CORTISONE IN THE ADRENOGENITAL SYNDROME ASSOCIATED WITH CONGENITAL ADRENAL HYPERPLASIA: AN ATTEMPT TO EXPLAIN AND CORRECT ITS DISORDERED HORMONAL PATTERN
... N., Wood, M., and Christo, E., Observations on adrenal cortical "sugar-fat-nitrogen" hormone "11-17-OCS" and "17-ketosteroid precursor" production by normal and abnormal individuals of v[r] ...
16
CHARACTERIZATION OF URINARY STEROIDS IN ADRENAL HYPERPLASIA: ISOLATION OF METABOLITES OF CORTISOL, COMPOUND S, AND DESOXYCORTICOSTERONE FROM A NORMOTENSIVE PATIENT WITH ADRENOGENITAL SYNDROME
... CHARACTERIZATION OF URINARY STEROIDS IN ADRENAL HYPERPLASIA: ISOLATION OF METABOLITES OF CORTISOL, COMPOUND S, AND DESOXYCORTICOSTERONE FROM A NORMOTENSIVE PATIENT WITH ADRENOGENITAL SYN[r] ...
15
CASE OF ADRENOGENITAL SYNDROME WITH HYPERTENSION TREATED WITH CORTISONE
... A., and Wilkins, L., Effect of adrenocorticotrophic hormone in congenital adrenal hyperplasia with virilism and in Cushing’s syndrome treated with methyl testosterone, J. B., Zygmuntowic[r] ...
11
THE ADRENOGENITAL SYNDROME WITH DEFICIENCY OF 3β HYDROXYSTEROID DEHYDROGENASE
... In those cases attributed to a deficiency of 3,8-hydroxysteroid dehydrogenase I-VI, the largest part of the steroids isolated and identified was comprised of compounds with A5-3,8-ol str[r] ...
8
DIFFICULTIES IN THE DIAGNOSIS OF THE ADRENOGENITAL SYNDROME IN INFANCY
... No pregnanetriol was de- tected in urine collected on the seventh day of life, and the major steroid excreted is. l6r-hydroxypregnenolone[r] ...
10
CLINICAL AND METABOLIC VARIATIONS IN THE ADRENOGENITAL SYNDROME
... found that the levels of pregnanetriol were extremely high in the unines of all patients witim vinihizing adrenal hyperplasia studied tip until that time, although no untreated. hyperten[r] ...
11
PSYCHOLOGIC STUDIES BEFORE AND AFTER CLITORIDECTOMY IN FEMALE PSEUDOHERMAPHRODITISM CAUSED BY CONGENITAL VIRILIZING ADRENAL HYPERPLASIA
... Results of this study indicate that by the age of 6 years, female pseudohermaphro- dites with the adrenogenital syndrome need not manifest significant disturbances of per- sonabity as me[r] ...
10
Neuroblastoma Associated With Adrenocortical Defects
... We recently reviewed the pathology of the adrenal medullas of two patients who had undergone bilateral adrenalectomy for uncontrolled adrenogenital syndrome and found no evidence of neur[r] ...
5
Extra Aneurysmal Flow Modification Following Pipeline Embolization Device Implantation: Focus on Regional Branches, Perforators, and the Parent Vessel
... RESULTS: Slow flow was observed in 13 of 68 (19.1%) side branches covered by the Pipeline Embolization Device. It was reported in all cases of anterior cerebral artery coverage, in 3/5 cases of M2-MCA coverage, and in ...
7
The Fifth Phakomatosis – A Case Report
... inherited syndrome manifested by multiple defects involving the skin, nervous system, eyes, endocrine system, and ...nevus syndrome, multiple basal cell carcinoma syndrome, Gorlin syndrome, or ...
5
Systemic Lupus Erythematosus: A Review
... hypertension syndrome, characterized by an elevated intracranial pressure, papilledema, and headache with occasional abducens nerve paresis, absence of a space-occupying lesion or ventricular enlargement, and ...
14
Download Download PDF
... FIGURE 1. Typical presentation of posterior reversible encephalop- athy syndrome. Brain computerized tomography demonstrates areas of a white matter hypodensity affecting symmetrically: Frontal lobes (A), and ...
7
The expanding spectrum of rare monogenic autoinflammatory diseases
... The mode of inheritance is dominant however many sporadic cases of porokeratosis have been described [47]. Mutations in the MeValonate Kinase ( MVK ) gene were found in DSAP patients [48,49]. The MVK enzyme is in- volved ...
12
Relative safety of steroid sparing agents in frequently relapsing, steroid dependent and steroid resistant nephrotic syndrome in pediatric patients
... nephrotic syndrome (FRNS), steroid-dependent nephrotic syndrome (SDNS) and steroid resistant nephrotic syndrome (SRNS) steroids are either used for prolonged period of time or ...
5
Significance of defecography and the role of rectocele in constipated patients
... Constipation is functionally separated into the follow- ing subgroups: slow colonic transit, normal colonic tran- sit, and defecatory or rectal evacuation abnormalities [2]. Disorders that are associated with pelvic ...
5