Opitz C syndrome and pseudohypoaldosteronism
- 1 December 1990
- journal article
- case report
- Published by Wiley in American Journal of Medical Genetics
- Vol. 37 (4) , 457-459
- https://doi.org/10.1002/ajmg.1320370405
Abstract
The C syndrome of multiple congenital anomalies is described in a male infant with pseudohypoaldosteronism. The association of these 2 rare autosomal recessive conditions is discussed.Keywords
This publication has 8 references indexed in Scilit:
- Cloning of Human Mineralocorticoid Receptor Complementary DNA: Structural and Functional Kinship with the Glucocorticoid ReceptorScience, 1987
- Aldosterone-Receptor Deficiency in PseudohypoaldosteronismNew England Journal of Medicine, 1985
- Trigonocephaly and the Opitz C syndrome.Journal of Medical Genetics, 1985
- Opitz trigonocephaly syndrome: Report of two casesEuropean Journal of Pediatrics, 1984
- Further delineation of the C (trigonocephaly) syndromeAmerican Journal of Medical Genetics, 1981
- FAMILIAL DOMINANT PSEUDOHYPOALDOSTERONISMThe Lancet, 1978
- The Nature of the Defect in a Salt-Wasting Disorder in Jews of Iran12Journal of Clinical Endocrinology & Metabolism, 1977
- The Opitz Trigonocephaly SyndromeAmerican Journal of Diseases of Children, 1975