Library

feed icon rss

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
  • 1
    ISSN: 1432-2072
    Keywords: Zimelidine ; ACTH ; Metyrapone ; Corticosteroids
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Plasma ACTH levels after oral ingestion of 2 g metyrapone at 24.00 hours in six healthy subjects were higher after pretreatment with zimelidine (300 mg) in comparison to placebo. Since zimelidine is a relatively selective serotonin reuptake inhibitor its action on hypothalamic-pituitaryadrenal (HPA) activity suggests that serotonin is a potent stimulator of ACTH release. The ratio of cortisol to 11-deoxycortisol was taken as a measure of 11-hydroxylase activity, which indicates biological activity of secreted ACTH. These cortisol/11-deoxycortisol ratios were significantly increased after zimelidine treatment, when compared to placebo. Both the ACTH response and the cortisol/11-deoxycortisol ratios substantiate evidence derived from animal experiments, indicating a stimulatory influence of serotonin on HPA activity. No firm conclusion, however, may be drawn on by which mechanism zimelidine exerts its action on the HPA-axis. Moreover these findings provide no information on whether serotonin has a stimulatory role on ACTH production under physiological condition.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Monatsschrift Kinderheilkunde 146 (1998), S. 678-682 
    ISSN: 1433-0474
    Keywords: Schlüsselwörter Vorzeitige Pubertät ; Gonadotropine ; Knochenreifung ; Wachstum ; GnRH-Agonist ; Key words Precocious puberty ; Gonadotropins ; Bone maturation ; Growth ; GnRH agonist
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Description / Table of Contents: Summary We report on two girls with atypical, self-remitting central precocious puberty and their subsequent development until (near) final height. Both showed thelarche prior to chronological age 4 years and an accelerated progressive bone maturation (delta bone age/delta chronological age 1.86 and 3.21, respectively). In patient 1, the hormonal find-ings were not typical for central precocious puberty (Gonadotropin-releasing-hormone-stimulated LH/FSH ratio 0.54, estradiol 14 pg/ml). In patient 2 the hormonal results were borderline (stimulated LH/FSH ratio 1.0, estradiol 〈5 pg/ml). During the next 5 years a spontaneous arrest of pubertal development was seen in patient 1 until normal puberty started at age 10 years (menarche 12.7 years). Patient 2 showed a complete regression of pubertal signs until now (age 8 years). Both patients were not treated. Patient 1 reached a normal adult height (168 cm). The remaining growth potential of patient 2 is favourable (height SDS for bone age). Discussion: A review of the literature on atyp-ical central precocious puberty showed that there is a continuum between the extremes of isolated premature thelarche on one end and of progressive central precocious puberty at the other end of the spectrum. This variability refers to the clinical appearance and also to bone maturation and hormonal findings. Even the progression of premature thelarche to overt central precocious puberty is possible. At initial evaluation a clear distinction between simple, non-progressive forms and aggressive, progressive forms is difficult. Thus, an observation period of several months before initiation of treatment is necessary in order to establish a correct diagnosis, the necessity to treat, and a correct evaluation of the efficacy of treatment.
    Notes: Zusammenfassung Zwei Mädchen mit atypisch verlaufender zentraler Pubertas praecox werden vorgestellt. Beide Patientinnen entwickelten die Thelarche vor dem 4. Lebensjahr. Sie zeigten eine akzelerierte und progrediente Knochenreifung (Δ Knochenalter/Δ chronologisches Alter 1,86 bzw. 3,21). Die Hormonbefunde von Patientin 1 waren nicht typisch für eine zentrale Pubertas praecox (stimulierter LH-FSH-Quotient 0,54, Östradiol 14 pg/ml). Die hormonelle Konstellation von Patientin 2 war grenzwertig (LH-FSH-Quotient 1,0, Östradiol 〈5 pg/ml). Bei Patientin 1 trat ein spontaner Stillstand der Pubertätsentwicklung ein. Die pubertäre Entwicklung setzte sich ab dem 10. Lebensjahr fort (Menarche mit 12,7 Jahren). Patientin 2 zeigte eine komplette Regression der Pubertätsentwicklung. Beide Patientinnen erhielten keine Therapie. Patientin 1 erreichte eine normale Endlänge (168 cm) im oberen Zielgrößenbereich. Das verbleibende Wachstumspotential von Patientin 2 ist gut (Längen-SDS für Knochenalter +0,5). Diskussion: Ein Überblick über die Literatur zeigt, daß es zwischen der isolierten prämaturen Thelarche und der progredienten Pubertas praecox vera als den beiden weithin bekannten diagnostischen Kategorien alle nur denkbaren Zwischenformen einer vorzeitigen Pubertätsentwicklung gibt. Diese Variabilität betrifft nicht nur das klinische Bild, sondern auch Knochenreifung und Hormonbefunde. Auch der Übergang einer prämaturen Thelarche in eine typische Pubertas praecox vera ist bekannt. Damit wird eine klare und eindeutige Trennung zwischen blanden und progredienten Verläufen schwierig. Eine Verlaufsbeobachtung von einigen Monaten vor Therapieeinleitung ist daher für die richtige Einordnung des Krankheitsbilds und damit für die Therapieindikation und die Beurteilung der Effektivität einer Behandlung unerläßlich.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 3
    Electronic Resource
    Electronic Resource
    Springer
    European journal of clinical pharmacology 18 (1980), S. 95-104 
    ISSN: 1432-1041
    Keywords: corticosteroids ; progestins ; betamethasone ; phenobarbital ; amniotic fluid ; fetoplacental unit
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Medicine
    Notes: Summary Corticosteroids (CS) are known to be essential for fetal organ maturation and seem to play an important role in both the initiation of parturition and the postnatal adaptation of the human neonate. Pharmacologically, CS are widely used for enhancing fetal lung maturation prior to premature delivery. However, knowledge of endogenous CS and precursor levels throughout fetal and perinatal life and their response to exogenous CS is limited. Therefore, using automated liquid column chromatography plus specific radioimmunoassays, unconjugated aldosterone (Aldo), corticosterone (B), 11-deoxycorticosterone (DOC), progesterone (P), 17-hydroxyprogesterone (17-OHP), 11-deoxycortisol (S), cortisol (F) and cortisone (E) were simultaneously followed in 70 amniotic fluid (AF) control samples throughout pregnancy, and in cord and neonatal plasma longitudinally during the first week of life. From 14 to 38 weeks, AF levels of all measured steroids except E rose by 2 to 12-fold on the average (allP〈0.001) but declined at term. E increased until 31–35 weeks (P〈0.01), then remained almost constant until term. Cord levels of all steroids were substantially higher than those found in AF at term. While levels of the placentally derived steroids P, 17-OHP, DOC and E dropped sharply after birth by several orders of magnitude (P≪0.01) showing typical disappearance curves, the biologically most potent CS Aldo and F rose even further immediately after birth. Whereas Aldo levels declined from maxima about 100 times above normal adult levels at 6 h by almost 3-fold until day 7 (P〈0.01), F (and also B) fluctuated considerably resembling a damped oscillation and, by day 7, reached mean levels less than half of those seen in later childhood. After betamethasone treatment of the mother, neonatal levels of Aldo and F were suppressed to 24–69% of normal until day 9, whereas those of the other steroids (except E) returned to normal during the first hours of life. Phenobarbital (PB) therapy of the mother led to decreased steroid levels in maternal and umbilical venous plasma at term, while umbilical arterial CS levels, notably those of Aldo and F (P〈0.02), were increased when compared with untreated controls, indicating a stimulation of the most potent CS in the fetus after PB. The significance of the findings in view of fetoplacental function and fetal organ maturation is briefly discussed.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 4
    Electronic Resource
    Electronic Resource
    Springer
    European journal of pediatrics 142 (1984), S. 286-289 
    ISSN: 1432-1076
    Keywords: Pseudohypoaldosteronism ; Down syndrome ; Salt wasting syndrome ; Resonium A
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract At 4 weeks of age, an infant with Down syndrome developed severe dehydration and salt loss with the typical features of pseudohypoaldosteronism (PHA). Plasma renin activity, 11-deoxycorticosterone, corticosterone and aldosterone levels were all increased severalfold over the normal range for age, thus excluding an adrenal biosynthetic defect. Clinical condition, hyponatraemia and hyperkalaemia could be rapidly normalised by the ion exchange resin Resonium A® administered first as enema and later orally (3 g/day). At that time, no further salt supplementation was necessary. At 18 months of age, Resonium A could be completely withdrawn with neither clinical deterioration nor electrolyte abnormalities. However at 31/2 years of age, plasma renin activity and aldosterone were still markedly elevated while precursor steroids were normal and the clinical condition satisfactory. No side effects were observed with the Resonium A® therapy. The combination of trisomy 21 and PHA is very unusual. Similarly, the successful treatment of severe renal salt loss during infancy by sodium supplementation and concomitant potassium withdrawal via an oral ion exchange resin has not yet been described and warrants further therapeutic trials.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 5
    ISSN: 1432-1076
    Keywords: Gonadotropin-releasing hormone agonist ; Decapeptyl ; Precocious puberty ; Growth
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract A total of 82 patients (74 girls, 8 boys) are presently participating in an international multicentre trial for treatment of central precocious puberty (CPP) with a slow release gonadotropin-releasing hormone (GnRH) agonist depot preparation: Decapeptyl-Depot (DD). Of these patients, 53 (3 boys) were previously untreated (group 1) and 29 (5 boys) have been treated before with either a short-acting GnRH analogue or cyproterone acetate (group 2). Fifty-one patients (44 girls, 7 boys) were treated with DD for 12 months or more. Basal plasma luteinizing hormone (LH) levels decreased in both groups after 1 year of therapy. The LH response to intravenous GnRH was reduced in both groups. Basal plasma follicle stimulating hormone (FSH) levels decreased in both groups. Stimulated FSH levels were reduced in both groups after 1 year of DD treatment. Plasma oestradiol levels in the girls decreased to prepubertal levels in both groups. In all patients the clinical signs of precocious gonadarche such as breast development and menstruations (girls) and an increased testis volume (boys), did not further progress and sometimes regressed in several patients. Growth velocity decreased in the girls of group 1 from 9.0±0.72cm/year (mean±SEM) in the last half-year before treatment to 6.3±0.50 in the first half-year of treatment (P〈0.01) and to 4.5±0.23 cm/year in the second half-year (P〈0.01). After 12 months a stabilization of growth velocity was observed. The ΔBA/ΔCA ratio decreased during treatment in this group of girls, resulting in an improvement of adult height prediction from 161.9±3.3 cm (mean±SEM) at the start to 164.1±3.5cm after 18 months of therapy (P〈0.05). No change of height prediction was observed in group 2. At present we consider one i.m. injection of DD every 4 weeks as the treatment of choice in children with CPP.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 6
    ISSN: 1432-1076
    Keywords: Key words     Chromosomal mosaicism ; Gonadal dysgenesis ; GnRH test ; Cell selection in vivo
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract      A comparison has been made of a case with 45,X/46,XX/ 47,XXX mosaicism with some 50 cases in the literature. A significant positive correlation was found between height standard deviation scores of mosaic patients from the literature and the frequency of cells with a normal chromosome constitution (n = 21, r s = 0.552, P 〈 0.01). In contrast, a significant negative correlation was seen between body height and the frequency of cells with a 45,X constitution (n = 21, r s = –0.594, P 〈 0.01). There was no significant correlation of height standard deviation score with the 47,XXX cell line (n = 21, r s = –0.353). A patient with a rare chromosomal mosaicism (45,X/46,XX/ 47,XXX) is described. The diagnosis was first made by chromosome analysis in amniotic cells. The patient showed no symptoms suggestive of Turner syndrome and growth followed the 75th height percentile. Basal and gonadotropin-releasing hormone stimulated gonadotropin levels normalized after age 4.8 years and did not subsequently return to hypergonadotropic levels. In blood lymphocytes, there was an increase in the frequency of cells with a normal chromosome constitution over 9 years. This in vivo cell selection is discussed. Chromosome analysis in skin fibroblasts showed the same triple mosaicism with a similar distribution of cell lines as in blood lymphocytes. In conclusion, statistical evidence was demonstrated that the severity of short stature is correlated with the distribution of cell lines in 45,X/46,XX/47,XXX mosaicism. This finding is of importance for the genetic counselling in cases of prenatal diagnosis of mosaic Turner syndrome.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 7
    Electronic Resource
    Electronic Resource
    Springer
    European journal of pediatrics 126 (1977), S. 97-102 
    ISSN: 1432-1076
    Keywords: Lactobezoar ; Abdominal tumour ; Dehydration
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract A case of lactobezoar is described in an eleven weeks old infant with a history of prolonged vomiting and constipation. The feeding history revealed no abnormalities, but unusually high environmental temperatures plus increased sweating may have been responsible for the formation of the gastric milk coagulum which presented as a firm epigastric tumour persisting for several weeks. An abdominal neuroblastoma was suspected but the correct diagnosis was established by a barium meal. Conservative therapy with parenteral fluids and gentle gastric lavage resulted in prompt disintegration of the lactobezoar. The 9 previously reported cases in the literature are briefly discussed.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 8
    Electronic Resource
    Electronic Resource
    Springer
    European journal of pediatrics 146 (1987), S. 561-564 
    ISSN: 1432-1076
    Keywords: Anorexia nervosa ; Growth ; Knemometry
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Recently a novel and non-invasive technique of lower leg length measurement (knemometry) was introduced. The method estimates the distance between heel and knee in the sitting child with an accuracy of 0.09 mm(SD). Two female patients with anorexia nervosa, aged 14:4 and 13:7 years, weighing minus 27 and minus 38% of normal weight for age, were measured repeatedly with this method within periods of 72 and 129 days during hospitalization und up to 133 days thereafter. During the first 40 days of hospitalization, patient 1 was measured 30 times and showed significant shrinkage of the lower leg length of −0.040 mm/day (P〈0.001). Over the remainder of her hospital stay her mean lower leg length increment still was much less (+0.036 mm/day) than that expected just by increase of soft tissue due to rapid weight gain (+0.126 kg/day). The second patient also showed significant shrinkage of lower leg length during a 4 month period after discharge from the hospital (−0.009 mm/day,P〈0.01). This is the first demonstration of long term lower leg shrinkage in children. Its origin remains unclear, but this shrinkage is clearly distinct from either arbitrary changes of lower leg length due to errors of measurement or changes of body diameters due to temporary alterations of soft tissue (i.e. during periods of weight loss). We speculate that progressive atrophic changes of the epiphyseal plates still open in both patients may account for the observed long term shrinkage of lower leg length.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 9
    ISSN: 1432-1076
    Keywords: Chromosomal mosaicism ; Gonadal dysgenesis GnRH test ; Cell selection in vivo
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract A comparison has been made of a case with 45,X/46,XX/47,XXX mosaicism with some 50 cases in the literature. A significant positive correlation was found between height standard deviation scores of mosaic patients from the literature and the frequency of cells with a normal chromosome constitution (n=21,r s =0.552,P〈0.01). In contrast, a significant negative correlation was seen between body height and the frequency of cells with a 45,X constitution (n=21,r s =−0.594,P〈0.01). There was no significant correlation of height standard deviation score with the 47,XXX cell line (n=21,r s =−0.353). A patient with a rare chromosomal mosaicism (45,X/46,XX/47,XXX) is described. The diagnosis was first made by chromosome analysis in amniotic cells. The patient showed no symptoms suggestive of Turner syndrome and growth followed the 75th height percentile. Basal and gonadotropin-releasing hormone stimulated gonadotropin levels normalized after age 4.8 years and did not subsequently return to hypergonadotropic levels. In blood lymphocytes, there was an increase in the frequency of cells with a normal chromosome constitution over 9 years. This in vivo cell selection is discussed. Chromosome analysis in skin fibroblasts showed the same triple mosaicism with a similar distribution of cell lines as in blood lymphocytes. In conclusion, statistical evidence was demonstrated that the severity of short stature is correlated with the distribution of cell lines in 45,X/46,XX/47,XXX mosaicism. This finding is of importance for the genetic counselling in cases of prenatal diagnosis of mosaic Turner syndrome.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 10
    Electronic Resource
    Electronic Resource
    Springer
    European journal of pediatrics 157 (1998), S. 378-381 
    ISSN: 1432-1076
    Keywords: Key words Congenital hypoaldosteronism ; Aldosterone synthase ; CYP11B2 gene ; CMO type II ; Mineralocorticoids
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Two boys presenting with infection-triggered, life-threatening salt-loss and hyperkalaemia were published in 1991 in the European Journal of Pediatrics. In both boys, the diagnosis of corticosterone methyl oxidase (CMO) deficiency type II has been established on the basis of determinations of plasma and urinary steroids. We had the opportunity to perform a molecular genetic study in one of the two boys. This boy had an elevated plasma 18-hydroxycorticosterone/aldosterone ratio which is pathognomonic for CMO deficiency type II. Sequence analysis of the CYP11B2 gene revealed a homozygous single base exchange in codon 185 of CYP11B2 causing an amino acid substitution Thr185Ile. Conclusion A Thr185Ile mutation in the CYP11B2 gene was found in a patient with CMO deficiency type II. This mutation may change the secondary structure of the enzyme leading to its decreased activity.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...