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polyhydramnios/κάλιο
Ο σύνδεσμος αποθηκεύεται στο πρόχειρο
Σελίδα 1 από 56 Αποτελέσματα
Increased urinary flow without development of polyhydramnios in response to prolonged hypoxia in the ovine fetus.
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Σύνδεση εγγραφή
OBJECTIVE
In the ovine fetus subjected to 24 hours of hypoxia, urinary flow is normal within a few hours from the onset of hypoxia and there is a maintained inhibition of swallowing. We hypothesized that 4 days of fetal hypoxia would lead to polyhydramnios.
METHODS
Five late-gestation fetal sheep
[Polyhydramnios, prematurity, dystrophy, polyuria, constipation, nephrocalcinosis and renal tumor: presentation of a classic tubulopathy].
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Σύνδεση εγγραφή
BACKGROUND
A diagnostic workup of a renal mass will rarely lead to the diagnosis of a tubulopathy. We would like to stress the importance of taking a detailed history and of evaluating these findings in the context of the clinical symptoms.
METHODS
A 3 year old boy with a renal mass, diagnosed due
[Neonatal Bartter disease diagnosed with the detection of a mutation of the KCNJ1 gene which codifies the synthesis of the renal ROMK1 potassium channel].
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Σύνδεση εγγραφή
We report clinical data of a female patient with Bartter's syndrome who was initially diagnosed with idiophatic hypercalciuria and, subsequently, with hyperprostaglandin E, syndrome. The patient was born after premature delivery with a history of polyhydramnios. During the first two years of life,
Severe pseudohypoaldosteronism in a pair of twins not associated with hydramnios.
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Σύνδεση εγγραφή
A pair of non-identical twins with severe pseudohypoaldosteronism (PHA) were followed over a period of 4 years. The diagnosis was based on dehydration, hyponatremia, hyperkalemia, high urine sodium/potassium ratios, and high serum concentrations of aldosterone and renin. Sweat and saliva electrolyte
Hyperechogenic kidneys and polyhydramnios associated with HNF1B gene mutation.
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Σύνδεση εγγραφή
HNF1B mutation is the leading cause of isolated hyperechogenic fetal kidneys with normal or moderately large size. Although most cases have normal amniotic fluid volume, some cases present with early oligohydramnios and renal failure associated with high perinatal mortality.
Here we report on seven
Biochemical composition of fluids for amnioinfusion during fetoscopy.
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Σύνδεση εγγραφή
OBJECTIVE
To evaluate which of the commercially available solutions is best suited for amnioinfusion during fetoscopy, based on resemblance with the biochemical properties of amniotic fluid.
METHODS
Amniotic fluid samples from 10 pregnancies were studied. Specimens were obtained from 5 pathologic
[The neonatal form of Bartter's syndrome: current findings in etiology and physiopathology].
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Σύνδεση εγγραφή
I. Time has come to distinguish "Bartter syndrome" from "Bartter disease". The latter is an autosomal recessive renal tubulopathy which manifests itself mostly during infancy and childhood. II. Bartter disease is caused neither by a primary renal potassium loss nor by a primary renal
Clinical presentation of genetically defined patients with hypokalemic salt-losing tubulopathies.
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Σύνδεση εγγραφή
OBJECTIVE
Hypokalemic salt-losing tubulopathies (Bartter-like syndromes) comprise a set of clinically and genetically distinct inherited renal disorders. Mutations in four renal membrane proteins involved in electrolyte reabsorption have been identified in these disorders: the furosemide-sensitive
Cantú syndrome: Findings from 74 patients in the International Cantú Syndrome Registry.
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Σύνδεση εγγραφή
Cantú syndrome (CS), first described in 1982, is caused by pathogenic variants in ABCC9 and KCNJ8, which encode the regulatory and pore forming subunits of ATP-sensitive potassium (KATP ) channels, respectively. Multiple case reports of affected individuals have described the various
Clinical and diagnostic features of Bartter and Gitelman syndromes.
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Σύνδεση εγγραφή
UNASSIGNED
Bartter and Gitelman syndromes are autosomal recessive disorders of renal tubular salt handling. Due to their rarity, limited long-term data are available to inform prognosis and management.
UNASSIGNED
Long-term longitudinal data were analysed for 45 children with pathogenic variants in
[Antenatal form of Bartter's syndrome].
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Σύνδεση εγγραφή
Six cases of tubular disorder of antenatal onset responsible for biological manifestations characteristic of Bartter syndrome and severe hypercalciuria are reported. In all six cases, severe hydramnios occurred during pregnancy between the 26th and 28th week after the last menstrual period. All six
Transient hyponatremia of prematurity caused by mild Bartter syndrome type II: a case report
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Σύνδεση εγγραφή
Background: Bartter syndrome subtypes are a group of rare renal tubular diseases characterized by impaired salt reabsorption in the tubule, specifically the thick ascending limb of Henle's loop. Clinically, they are characterized by the
Genotype-phenotype correlations in normotensive patients with primary renal tubular hypokalemic metabolic alkalosis.
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Σύνδεση εγγραφή
Among the different forms of hereditary renal tubulopathies associated with hypokalemia, metabolic alkalosis and normotension, two main types of disorders have been identified: Gitelman disease, which appears to be a homogeneous post-Henle's loop disorder, and Bartter syndrome, a heterogeneous Henle
Pseudo-Bartter syndrome in an infant with congenital chloride diarrhoea.
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Σύνδεση εγγραφή
BACKGROUND
Pseudo-Bartter syndrome encompasses a heterogenous group of disorders similar to Bartter syndrome. We are presenting an infant with pseudo-Bartter syndrome caused by congenital chloride diarrhoea.
METHODS
A male newborn born in the 37th gestational week (GW) to young healthy and
A new method for selective reduction in TRAP sequence with a contraindication to fetoscopic surgery: A case report.
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Σύνδεση εγγραφή
BACKGROUND
The preferred method for multifetal pregnancy reduction (MFPR) is a transabdominal intrathoracic or intracranial injection of potassium chloride (KCl). However, in monochorionic multiple pregnancies (MMPs), especially in monoamnionic multifetal pregnancies, selective feticide by this
Η πληρέστερη βάση δεδομένων φαρμακευτικών βοτάνων που υποστηρίζεται από την επιστήμη
- Λειτουργεί σε 55 γλώσσες
- Βοτανικές θεραπείες που υποστηρίζονται από την επιστήμη
- Αναγνώριση βοτάνων με εικόνα
- Διαδραστικός χάρτης GPS - ετικέτα βότανα στην τοποθεσία (σύντομα)
- Διαβάστε επιστημονικές δημοσιεύσεις που σχετίζονται με την αναζήτησή σας
- Αναζήτηση φαρμακευτικών βοτάνων με τα αποτελέσματά τους
- Οργανώστε τα ενδιαφέροντά σας και μείνετε ενημερωμένοι με την έρευνα ειδήσεων, τις κλινικές δοκιμές και τα διπλώματα ευρεσιτεχνίας
Πληκτρολογήστε ένα σύμπτωμα ή μια ασθένεια και διαβάστε για βότανα που μπορεί να βοηθήσουν, πληκτρολογήστε ένα βότανο και δείτε ασθένειες και συμπτώματα κατά των οποίων χρησιμοποιείται.
* Όλες οι πληροφορίες βασίζονται σε δημοσιευμένη επιστημονική έρευνα
