PRENATAL DIAGNOSIS OF BARTTER SYNDROME

The Lancet

Volumn 329, Issue 8529, 1987, Pages 394-

  Proesmans, W ^a   Massa, G ^a   Vandenberghe, K ^a   Van Assche, A ^a  

^a UNIVERSITY HOSPITALS LEUVEN   (Belgium)

Author keywords

[No Author keywords available]

Indexed keywords

ELECTROLYTE;

AMNION FLUID; BARTTER SYNDROME; CONGENITAL DISORDER; DIAGNOSIS; FETUS; HUMAN; HUMAN CELL; HYDRAMNIOS; KIDNEY; PREGNANCY; PRENATAL DIAGNOSIS; PRIORITY JOURNAL;

AMNIOTIC FLUID; BARTTER'S DISEASE; ELECTROLYTES; FEMALE; FETAL DISEASES; HUMAN; HYPERALDOSTERONISM; PREGNANCY; PRENATAL DIAGNOSIS;

EID: 0023151480     PISSN: 01406736     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0140-6736(87)91781-8     Document Type: Letter

References (4)

1. Hyperplasia of the juxtaglomerular complex with hyperaldosteronism and hypokalemic alkalosis
2. Barner's syndrome: differentiation into two clinical groups
3. A variant of Bartter's syndrome: Bartter's syndrome associated with hydramnios, prematurity, hypercalciuria and nephrocalcinosis
4. Bartter syndrome in two siblings—antenatal and neonatal observations