aldosterone has been researched along with Failure to Thrive in 10 studies
Failure to Thrive: A condition of substandard growth or diminished capacity to maintain normal function.
| Excerpt | Relevance | Reference |
|---|---|---|
| "Pseudohypoaldosteronism type I is a rare genetic disease of mineralocorticoid resistance that typically manifests in neonatal age." | 1.56 | Failure to Thrive, Hyponatremia, Hyperkalemia - Differential Diagnostic Reflections of a Rare Genetic Disease. ( de Potzolli, B; Seeliger, S; Tropschuh, A, 2020) |
| "Failure to thrive was the most common symptom with hyponatraemia on presentation." | 1.46 | Transient pseudohypoaldosteronism in infancy secondary to urinary tract infection. ( Abraham, MB; Choong, CS; Larkins, N; Shetty, VB, 2017) |
| "Failure to thrive was noted in five of the six patients." | 1.39 | Clinical and molecular analysis of six Japanese patients with a renal form of pseudohypoaldosteronism type 1. ( Abe, M; Hamajima, T; Hara, S; Hatta, Y; Iwata, J; Kamijo, T; Nakamura, A; Okada, M; Tajima, T; Tsuyuki, K; Ushio, M, 2013) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 2 (20.00) | 18.7374 |
| 1990's | 1 (10.00) | 18.2507 |
| 2000's | 1 (10.00) | 29.6817 |
| 2010's | 5 (50.00) | 24.3611 |
| 2020's | 1 (10.00) | 2.80 |
| Authors | Studies |
|---|---|
| Tropschuh, A | 1 |
| de Potzolli, B | 1 |
| Seeliger, S | 1 |
| Tanaka, T | 1 |
| Oki, E | 1 |
| Mori, T | 1 |
| Tsuruga, K | 1 |
| Sohara, E | 1 |
| Uchida, S | 1 |
| Tanaka, H | 1 |
| Sopfe, J | 1 |
| Simmons, JH | 1 |
| Abraham, MB | 1 |
| Larkins, N | 1 |
| Choong, CS | 1 |
| Shetty, VB | 1 |
| Hubert, EL | 1 |
| Teissier, R | 1 |
| Fernandes-Rosa, FL | 1 |
| Fay, M | 1 |
| Rafestin-Oblin, ME | 1 |
| Jeunemaitre, X | 1 |
| Metz, C | 1 |
| Escoubet, B | 1 |
| Zennaro, MC | 1 |
| Hatta, Y | 1 |
| Nakamura, A | 1 |
| Hara, S | 1 |
| Kamijo, T | 1 |
| Iwata, J | 1 |
| Hamajima, T | 1 |
| Abe, M | 1 |
| Okada, M | 1 |
| Ushio, M | 1 |
| Tsuyuki, K | 1 |
| Tajima, T | 1 |
| Maruyama, K | 1 |
| Watanabe, H | 1 |
| Onigata, K | 1 |
| Schindler, AM | 1 |
| Bergman, GE | 1 |
| Buchta, RM | 1 |
| Picco, P | 1 |
| Garibaldi, L | 1 |
| Cotellessa, M | 1 |
| DiRocco, M | 1 |
| Borrone, C | 1 |
1 review available for aldosterone and Failure to Thrive
| Article | Year |
|---|---|
Failure to thrive, hyponatremia, and hyperkalemia in a neonate.
Topics: Aldosterone; Diagnosis, Differential; Failure to Thrive; Humans; Hyperkalemia; Hyponatremia; Infant, | 2013 |
9 other studies available for aldosterone and Failure to Thrive
| Article | Year |
|---|---|
Failure to Thrive, Hyponatremia, Hyperkalemia - Differential Diagnostic Reflections of a Rare Genetic Disease.
Topics: Adult; Aldosterone; Child, Preschool; Diagnosis, Differential; Failure to Thrive; Humans; Hyperkalem | 2020 |
Complete clinical resolution of a Japanese family with renal pseudohypoaldosteronism type 1 due to a novel NR3C2 mutation.
Topics: Age Factors; Aldosterone; Child, Preschool; Failure to Thrive; Genetic Association Studies; Humans; | 2019 |
Transient pseudohypoaldosteronism in infancy secondary to urinary tract infection.
Topics: Aldosterone; Failure to Thrive; Follow-Up Studies; Humans; Hyponatremia; Infant; Male; Pseudohypoald | 2017 |
Mineralocorticoid receptor mutations and a severe recessive pseudohypoaldosteronism type 1.
Topics: Aldosterone; Animals; Child, Preschool; Chlorocebus aethiops; Codon, Nonsense; Codon, Terminator; CO | 2011 |
Clinical and molecular analysis of six Japanese patients with a renal form of pseudohypoaldosteronism type 1.
Topics: Aldosterone; Failure to Thrive; Female; Heterozygote; Humans; Infant; Infant, Newborn; Japan; Kidney | 2013 |
Reversible secondary pseudohypoaldosteronism due to pyelonephritis.
Topics: Acute Disease; Aldosterone; Failure to Thrive; Humans; Hyperkalemia; Hyponatremia; Infant; Male; Phi | 2002 |
Hyponatremia in a baby who refused to nurse.
Topics: Aldosterone; Breast Feeding; Failure to Thrive; Female; Humans; Hyponatremia; Infant; Renin-Angioten | 1984 |
Type 2 corticosterone methyloxidase defect in a 2-year-old Iranian Jewish child.
Topics: Aldosterone; Child, Preschool; Cytochrome P-450 CYP11B2; Failure to Thrive; Humans; Iran; Jews; Male | 1984 |
Corticosterone methyl oxidase type II deficiency: a cause of failure to thrive and recurrent dehydration in early infancy.
Topics: 18-Hydroxycorticosterone; Aldosterone; Cytochrome P-450 CYP11B2; Dehydration; Diagnosis, Differentia | 1992 |