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Biomedical subjects

G B Stoelinga

Publications and source records attributed to G B Stoelinga.

At least 55 records · Page 3Linked to original sources

Salivary and plasma androstenedione and 17-hydroxyprogesterone levels in congenital adrenal hyperplasia.

Androstenedione (A-dione) and 17-hydroxyprogesterone (17-OHP) levels were measured in matched samples of saliva and of plasma collected from patients with congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency (eight patients) and 11-hydroxylase deficiency (one patient). Positive correlations were found between salivary and plasma values of either steroid with correlation coefficients of 0.968 for A-dione and 0.935 for 17-OHP. All five inadequately treated patients with 21-hydroxylase deficiency had greatly elevated plasma and salivary 17-OHP concentrations compared to values in age matched controls. In two of three well controlled patients plasma 17-OHP levels were less than 40 nmol/liter and salivary levels were less than 1.5 nmol/liter, the upper limits which have been formulated as a guideline for monitoring control in treated CAH patients. Patients in good control had A-dione levels in plasma (0.6-2.2 nmol/liter) and saliva (0.04-0.15 nmol/liter) which were both within the normal range for prepubertal children (0.14-2.40 nmol/liter and 0.02-0.25 nmol/liter respectively). Patients in poor control had A-dione levels in plasma of 5.2-25.4 nmol and in saliva of 0.50-2.21 nmol/liter. These values exceeded without exception the normal ranges for their respective ages. Salivary A-dione and 17-OHP determinations are a useful adjunct in the diagnosis and the monitoring of CAH patients since they can be obtained easily and nonstressfully.

17-alpha-Hydroxyprogesterone↗

Ultrasound detection of congenital arteriovenous aneurysm of the great cerebral vein of Galen.

Using combined echoencephalography and Doppler flow determination the diagnosis Arteriovenous aneurysm of the great cerebral vein of Galen could be made in two infants. Without vascular surgery one patient died, the other recovered completely. CT scanning confirmed the diagnosis. Invasive methods such as cerebral angiography were avoided. Case histories, neuropathological findings, ultrasound method and results are presented. Pathogenesis, clinical signs, treatment and prognosis are discussed. With the ultrasound method presented, the nature and location of the vascular anomaly were demonstrable, thus additional higher risk diagnostic methods could be avoided or planned more purposefully.

Autopsy↗

Doppler flow characteristics in the main pulmonary artery and the LA/Ao ratio before and after ductal closure in healthy newborns.

Echo-Doppler (ED) techniques were used to estimate the time of closure of the ductus arteriosus in 30 normal neonates. We found that after birth there was a left-to-right (L-R) shunt through the ductus, which disappeared within 14 hours in 50% of the neonates investigated. Furthermore, patency of the ductus was not associated with a murmur. After closure of the ductus there was a significant diminution of the echocardiographically determined left atrium/aortic (LA/Ao) ratio, which was used as a measure of the L-R shunt.

Blood Circulation↗