Page last updated: 2024-11-07

aldosterone and Spasms, Infantile

aldosterone has been researched along with Spasms, Infantile in 1 studies

Spasms, Infantile: An epileptic syndrome characterized by the triad of infantile spasms, hypsarrhythmia, and arrest of psychomotor development at seizure onset. The majority present between 3-12 months of age, with spasms consisting of combinations of brief flexor or extensor movements of the head, trunk, and limbs. The condition is divided into two forms: cryptogenic (idiopathic) and symptomatic (secondary to a known disease process such as intrauterine infections; nervous system abnormalities; BRAIN DISEASES, METABOLIC, INBORN; prematurity; perinatal asphyxia; TUBEROUS SCLEROSIS; etc.). (From Menkes, Textbook of Child Neurology, 5th ed, pp744-8)

Research

Studies (1)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (100.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Radetti, G1
Rizza, F1
Mengarda, G1
Pittschieler, K1

Other Studies

1 other study available for aldosterone and Spasms, Infantile

ArticleYear
Adipsic hypernatremia in two sisters.
    American journal of diseases of children (1960), 1991, Volume: 145, Issue:3

    Topics: Aldosterone; Blood Urea Nitrogen; Female; Humans; Hypernatremia; Hypothalamus; Inappropriate ADH Syn

1991