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aldosterone and Inborn Errors of Metabolism

aldosterone has been researched along with Inborn Errors of Metabolism in 57 studies

Research Excerpts

ExcerptRelevanceReference
"Forms of congenital adrenal hyperplasia resulting from deficient steroid hydroxylation at positions 21, 17 alpha, and 11 beta have several similar clinical and biochemical characteristics."5.27Distinctive plasma aldosterone, 18-hydroxycorticosterone, and 18-hydroxydeoxycorticosterone profile in the 21-, 17 alpha-, and 11 beta-hydroxylase deficiency types of congenital adrenal hyperplasia. ( Biglieri, EG; Kater, CE, 1983)
"Low-renin hypertension affects 30% of hypertensive patients."2.61Low-Renin Hypertension. ( Athimulam, S; Bancos, I; Lazik, N, 2019)
"Forms of congenital adrenal hyperplasia resulting from deficient steroid hydroxylation at positions 21, 17 alpha, and 11 beta have several similar clinical and biochemical characteristics."1.27Distinctive plasma aldosterone, 18-hydroxycorticosterone, and 18-hydroxydeoxycorticosterone profile in the 21-, 17 alpha-, and 11 beta-hydroxylase deficiency types of congenital adrenal hyperplasia. ( Biglieri, EG; Kater, CE, 1983)
"Aldosterone deficiency was due to an inborn error selectively involving the terminal portion of the bio-synthetic pathway and characterized by an enzymic block in the conversion of 18-hydroxy-corticosterone to aldosterone."1.26Selective hypoaldosteronism in Iranian Jews: An autosomal recessive trait. ( Cohen, T; Rösler, A; Theodor, R, 1977)
"Aldosterone deficiency was due to an inborn error involving the terminal portion of the biosynthetic pathway and characterized by marked overproduction of glomerulosa zone 18-hydroxycorticosterone relative to aldosterone."1.26The nature of the defect in a salt-wasting disorder in Jews of Iran. ( Rabinowitz, D; Ramirez, LC; Rösler, A; Theodor, R; Ulick, S, 1977)

Research

Studies (57)

TimeframeStudies, this research(%)All Research%
pre-199048 (84.21)18.7374
1990's6 (10.53)18.2507
2000's0 (0.00)29.6817
2010's3 (5.26)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Athimulam, S1
Lazik, N1
Bancos, I1
Chiang, JK1
Chen, CL1
Tseng, FY1
Chi, YC1
Huang, KC1
Yang, WS1
Donner, KM1
Hiltunen, TP1
Jänne, OA1
Sane, T1
Kontula, K1
MCARDLE, B1
VISSER, HK4
DEGENHART, HJ1
COST, WS3
CROUGHS, W1
ULICK, S7
GAUTIER, E1
VETTER, KK1
MARKELLO, JR1
YAFFE, S1
LOWE, CU1
BRYAN, GT1
KLIMAN, B1
BARTTER, FC1
KOWARSKI, A1
FINKELSTEIN, JW1
SPAULDING, JS1
HOLMAN, GH1
MIGEON, CJ1
Veldhuis, JD1
Melby, JC1
Kater, CE1
Biglieri, EG2
Frézal, J1
Honour, JW1
Dillon, MJ1
Shackleton, CH1
Brautbar, C1
Theodor, R4
Sack, J2
Levene, C1
Dupont, B1
Levine, LS1
Sharon, R1
Smaller, S1
Cohen, T2
Rösler, A5
Funder, JW1
Yong, AB1
Montalto, J1
Pitt, J1
Oakes, S1
Preston, T1
Buchanan, C1
Shizuta, Y1
Kawamoto, T1
Mitsuuchi, Y1
Miyahara, K1
Imura, H1
Fuller, PJ1
Lim-Tio, S1
Michelis, MF1
Murdaugh, HV1
Boichis, H1
Gerty, R1
Alagem, M1
Tabachinik, E1
Cohen, B1
Rabinowitz, D2
Katznelson, D1
Kraiem, Z1
Lunenfeld, B1
Holmberg, C1
Ramirez, LC1
Brautbar, N1
Litwin, JJ1
Wang, JZ1
Morton, DH1
Tedde, R1
Mantero, F1
Lee, PD1
Patterson, BD1
Hintz, RL1
Rosenfeld, RG1
Kenny, FM1
Reynolds, JW1
Green, OC1
Sassard, J1
Loras, B2
Poncet, J1
Vincent, M1
Gharib, C1
Miura, K1
Yoshinaga, K1
Goto, K1
Katsushima, I1
Maebashi, M1
Demura, H1
Iino, M1
Demura, R1
Torikai, T1
Lim, NY1
Mimica, N1
Dingman, JF1
Endo, J2
Kono, T3
Yoshimi, T2
Boyd, GW1
Peart, WS1
Schambelan, M1
Stockigt, JR1
Sizonenko, PC1
Riondel, AM1
Kohlberg, IJ1
Paunier, L1
Thistlethwaite, D1
Darling, JA1
Fraser, R1
Rees, LH1
Harkness, RA1
Fukuchi, S1
Nakajima, K1
Takenouchi, T1
Nishisato, K1
Hammerstein, J1
Zielske, F1
Dsitler, A1
Wolff, HP1
Graef, V1
de Lange, WE1
Weeke, A1
Artz, W1
Jansen, W1
Doorenbos, H1
Yoshida, H1
Shimizu, N1
David, RR1
Asnis, M1
Drucker, WD1
Kaplan, NM1
Strickland, AL1
Kotchen, TA1
Murphy, BE1
Haour, F1
Bertrand, J1
Klevit, HD1
Rappaport, R1
Dray, F1
Legrand, JC1
Royer, P1
Vagnucci, AH1
Bejar, RL1
Cleveland, WW1

Reviews

9 reviews available for aldosterone and Inborn Errors of Metabolism

ArticleYear
Low-Renin Hypertension.
    Endocrinology and metabolism clinics of North America, 2019, Volume: 48, Issue:4

    Topics: Aldosterone; Citrus paradisi; Cushing Syndrome; Glycyrrhiza; Humans; Hyperaldosteronism; Hypertensio

2019
METABOLIC MYOPATHIES. THE GLYCOGENOSES AFFECTING MUSCLE, AND HYPO- AND HYPERKALEMIC PERIODIC PARALYSIS.
    The American journal of medicine, 1963, Volume: 35

    Topics: Aldosterone; Carbohydrate Metabolism; Glucose-6-Phosphatase; Glucosidases; Glycogen Storage Disease;

1963
Isolated aldosterone deficiency in man: acquired and inborn errors in the biosynthesis or action of aldosterone.
    Endocrine reviews, 1981,Fall, Volume: 2, Issue:4

    Topics: 18-Hydroxycorticosterone; 18-Hydroxydesoxycorticosterone; Adrenal Glands; Adrenocorticotropic Hormon

1981
The promiscuous receptor: a case for the guardian enzyme.
    Cardiovascular research, 1995, Volume: 30, Issue:2

    Topics: 11-beta-Hydroxysteroid Dehydrogenases; Aldosterone; Animals; Corticosterone; Humans; Hydroxysteroid

1995
[17-alpha-hydroxylase deficiency].
    Nihon rinsho. Japanese journal of clinical medicine, 1971, Volume: 29, Issue:3

    Topics: Adolescent; Adrenal Cortex Hormones; Adrenocortical Hyperfunction; Adrenocorticotropic Hormone; Adul

1971
The relationship between angiotensin and aldosterone.
    Advances in metabolic disorders, 1971, Volume: 5

    Topics: Adrenal Gland Neoplasms; Aldosterone; Alkalosis; Angiotensin II; Animals; Humans; Hyperaldosteronism

1971
[Enzyme defects in steroid hormone biosynthesis].
    Deutsche medizinische Wochenschrift (1946), 1973, Jun-29, Volume: 98, Issue:26

    Topics: Adrenal Cortex Hormones; Adrenal Glands; Adrenal Hyperplasia, Congenital; Aldosterone; Estrogens; Fe

1973
[Recent knowledge of diseases with abnormal aldosterone secretion].
    Naika hokan. Japanese archives of internal medicine, 1971, Volume: 18, Issue:1

    Topics: Addison Disease; Adolescent; Adrenal Cortex Hormones; Adrenal Gland Neoplasms; Adult; Aldosterone; A

1971
[Aldosterone deficiency].
    Nihon rinsho. Japanese journal of clinical medicine, 1971, Volume: 29, Issue:3

    Topics: Adult; Aldosterone; Autonomic Nervous System; Endocrine System Diseases; Heart Failure; Heparin; Hum

1971

Other Studies

48 other studies available for aldosterone and Inborn Errors of Metabolism

ArticleYear
Higher blood aldosterone level in metabolic syndrome is independently related to adiposity and fasting plasma glucose.
    Cardiovascular diabetology, 2015, Jan-13, Volume: 14

    Topics: Adiponectin; Adiposity; Aldosterone; Biomarkers; Blood Glucose; Cross-Sectional Studies; Fasting; Fe

2015
Generalized glucocorticoid resistance caused by a novel two-nucleotide deletion in the hormone-binding domain of the glucocorticoid receptor gene NR3C1.
    European journal of endocrinology, 2013, Volume: 168, Issue:1

    Topics: Adult; Aldosterone; Animals; Base Sequence; Coronary Artery Disease; COS Cells; Female; Frameshift M

2013
ADRENOCORTICAL CONTROL OF RENAL SODIUM AND POTASSIUM EXCRETION IN THE NEWBORN PERIOD.
    Maandschrift voor kindergeneeskunde, 1964, Volume: 32

    Topics: 17-Hydroxycorticosteroids; Adrenal Glands; Adrenocortical Hyperfunction; Adrenocorticotropic Hormone

1964
AN ALDOSTERONE BIOSYNTHETIC DEFECT IN A SALT-LOSING DISORDER.
    The Journal of clinical endocrinology and metabolism, 1964, Volume: 24

    Topics: Addison Disease; Adrenal Cortex Hormones; Adrenal Insufficiency; Adrenocortical Hyperfunction; Aldos

1964
[HEREDITARY DISORDERS IN ALDOSTERONE AND HYDROCORTISONE SYNTHESIS].
    Nederlands tijdschrift voor geneeskunde, 1964, Sep-19, Volume: 108

    Topics: Aldosterone; Humans; Hydrocortisone; Infant; Infant, Newborn; Metabolism, Inborn Errors

1964
[A NEW HEREDITARY ENZYME DEFECT IN ALDOSTERONE SYNTHESIS (18-OXIDATION DEFECT)].
    Nederlands tijdschrift voor geneeskunde, 1964, Oct-24, Volume: 108

    Topics: Adrenal Hyperplasia, Congenital; Adrenocorticotropic Hormone; Adrenogenital Syndrome; Aldosterone; B

1964
A NEW HEREDITARY DEFECT IN THE BIOSYNTHESIS OF ALDOSTERONE: URINARY C21-CORTICOSTEROID PATTERN IN THREE RELATED PATIENTS WITH A SALT-LOSING SYNDROME, SUGGESTING AN 18-OXIDATION DEFECT.
    Acta endocrinologica, 1964, Volume: 47

    Topics: 17-Hydroxycorticosteroids; 17-Ketosteroids; Adolescent; Adrenal Cortex Hormones; Adrenocorticotropic

1964
IMPAIRED ALDOSTERONE PRODUCTION IN "SALT-LOSING" CONGENITAL ADRENAL HYPERPLASIA.
    The Journal of clinical investigation, 1965, Volume: 44

    Topics: Adrenal Hyperplasia, Congenital; Adrenogenital Syndrome; Aldosterone; Child; Chromatography; Humans;

1965
ALDOSTERONE SECRETION RATE IN CONGENITAL ADRENAL HYPERPLASIA. A DISCUSSION OF THE THEORIES ON THE PATHOGENESIS OF THE SALT-LOSING FORM OF THE SYNDROME.
    The Journal of clinical investigation, 1965, Volume: 44

    Topics: Adolescent; Adrenal Hyperplasia, Congenital; Adrenogenital Syndrome; Aldosterone; Bodily Secretions;

1965
Distinctive plasma aldosterone, 18-hydroxycorticosterone, and 18-hydroxydeoxycorticosterone profile in the 21-, 17 alpha-, and 11 beta-hydroxylase deficiency types of congenital adrenal hyperplasia.
    The American journal of medicine, 1983, Volume: 75, Issue:1

    Topics: 18-Hydroxycorticosterone; 18-Hydroxydesoxycorticosterone; Adolescent; Adrenal Hyperplasia, Congenita

1983
[Pseudohypoaldosteronism: a new family].
    Archives francaises de pediatrie, 1983, Volume: 40, Issue:8

    Topics: Aldosterone; Female; Humans; Infant; Metabolism, Inborn Errors; Natriuresis

1983
Analysis of steroids in urine for differentiation of pseudohypoaldosteronism and aldosterone biosynthetic defect.
    The Journal of clinical endocrinology and metabolism, 1982, Volume: 54, Issue:2

    Topics: Aldosterone; Child, Preschool; Chromatography, Gas; Corticosterone; Diagnosis, Differential; Female;

1982
HLA in a selective aldosterone biosynthetic defect due to type 2 corticosterone methyl-oxidase deficiency.
    Tissue antigens, 1981, Volume: 17, Issue:2

    Topics: Aldosterone; Consanguinity; Cytochrome P-450 CYP11B2; Female; Genes, Recessive; Genetic Linkage; Hap

1981
Corticosterone methyl oxidase type II (CMO II) deficiency: biochemical approach to diagnosis.
    Clinical biochemistry, 1994, Volume: 27, Issue:6

    Topics: 18-Hydroxycorticosterone; Aldosterone; Cytochrome P-450 CYP11B2; Diagnosis, Differential; Fludrocort

1994
Inborn errors of aldosterone biosynthesis in humans.
    Steroids, 1995, Volume: 60, Issue:1

    Topics: Adrenal Hyperplasia, Congenital; Aldosterone; Amino Acid Sequence; Base Sequence; Cytochrome P-450 C

1995
Aldosterone action, sodium channels and inherited disease.
    The Journal of endocrinology, 1996, Volume: 148, Issue:3

    Topics: Aldosterone; Epithelium; Humans; Hypertension; Hypokalemia; Metabolism, Inborn Errors; Mineralocorti

1996
Selective hypoaldosteronism. An editorial revisited after 15 years.
    The American journal of medicine, 1975, Volume: 59, Issue:1

    Topics: Adrenal Glands; Adrenocorticotropic Hormone; Aldosterone; Angiotensin II; Arrhythmias, Cardiac; Hear

1975
Metabolic responses to the administration of angiotensin II, K and ACTH in two salt-wasting syndromes.
    The Journal of clinical endocrinology and metabolism, 1977, Volume: 44, Issue:2

    Topics: Adrenocorticotropic Hormone; Aldosterone; Angiotensin II; Child, Preschool; Diet; Female; Humans; Hy

1977
Management of congenital hypoaldosteronism.
    Monographs in human genetics, 1978, Volume: 10

    Topics: Adrenocorticotropic Hormone; Aldosterone; Body Height; Desoxycorticosterone; Humans; Hydrocortisone;

1978
Electrolyte economy and its hormonal regulation in congenital chloride diarrhea.
    Pediatric research, 1978, Volume: 12, Issue:2

    Topics: Adolescent; Aldosterone; Child; Child, Preschool; Chlorides; Diarrhea; Electrolytes; Extracellular S

1978
Selective hypoaldosteronism in Iranian Jews: An autosomal recessive trait.
    Clinical genetics, 1977, Volume: 11, Issue:1

    Topics: Aldosterone; Female; Genes, Recessive; Humans; Iran; Jews; Male; Metabolism, Inborn Errors; Pedigree

1977
The nature of the defect in a salt-wasting disorder in Jews of Iran.
    The Journal of clinical endocrinology and metabolism, 1977, Volume: 44, Issue:2

    Topics: Adolescent; Adult; Aldosterone; Blood Urea Nitrogen; Body Height; Body Weight; Carbon Dioxide; Child

1977
Diagnosis and nomenclature of the disorders of the terminal portion of the aldosterone biosynthetic pathway.
    The Journal of clinical endocrinology and metabolism, 1976, Volume: 43, Issue:1

    Topics: 18-Hydroxycorticosterone; Adult; Aldosterone; Child; Child, Preschool; Corticosterone; Female; Human

1976
[Urinary salt wastage in the adult: a form of pseudohypoaldosteronism].
    Harefuah, 1976, Oct-01, Volume: 91, Issue:7

    Topics: Aldosterone; Female; Humans; Metabolism, Inborn Errors; Pedigree; Renal Tubular Transport, Inborn Er

1976
The biochemical phenotypes of two inborn errors in the biosynthesis of aldosterone.
    The Journal of clinical endocrinology and metabolism, 1992, Volume: 74, Issue:6

    Topics: 18-Hydroxycorticosterone; Adolescent; Adrenal Cortex Hormones; Adult; Aldosterone; Child; Child, Pre

1992
Pathogenesis of the type 2 variant of the syndrome of apparent mineralocorticoid excess.
    The Journal of clinical endocrinology and metabolism, 1990, Volume: 70, Issue:1

    Topics: Adult; Aldosterone; Cortisone; Dexamethasone; Female; Humans; Hydrocortisone; Male; Metabolism, Inbo

1990
Biochemical diagnosis and management of corticosterone methyl oxidase type II deficiency.
    The Journal of clinical endocrinology and metabolism, 1986, Volume: 62, Issue:1

    Topics: Adrenal Cortex Hormones; Aldosterone; Cytochrome P-450 CYP11B2; Female; Fludrocortisone; Genetic Car

1986
Partial 3 -hydroxysteroid dehydrogenase (3 -HSD) deficiency in a family with congenital adrenal hyperplasia: evidence for increasing 3 -HSD activity with age.
    Pediatrics, 1971, Volume: 48, Issue:5

    Topics: 17-Hydroxycorticosteroids; 17-Ketosteroids; Adrenal Gland Diseases; Aging; Aldosterone; Androstanes;

1971
[Study of renin activity and aldosterone secretion in adrenal hyperplasia due to 21-hydroxylase deficiency].
    Comptes rendus des seances de la Societe de biologie et de ses filiales, 1969, Volume: 163, Issue:6

    Topics: Adrenal Gland Diseases; Aldosterone; Child; Dexamethasone; Diet, Sodium-Restricted; Female; Humans;

1969
A case of glucocorticoid-responsive hyperaldosteronism.
    The Journal of clinical endocrinology and metabolism, 1968, Volume: 28, Issue:12

    Topics: 17-Hydroxycorticosteroids; Adolescent; Adrenal Glands; Adrenocorticotropic Hormone; Aldosterone; Blo

1968
Hyperaldosteronism in hypertensive congenital adrenal hyperplasia.
    The Journal of clinical endocrinology and metabolism, 1969, Volume: 29, Issue:12

    Topics: 17-Hydroxycorticosteroids; 17-Ketosteroids; Adrenal Hyperplasia, Congenital; Adrenal Rest Tumor; Adr

1969
Isolated hypoaldosteronism in adults. A renin-deficiency syndrome.
    The New England journal of medicine, 1972, Sep-21, Volume: 287, Issue:12

    Topics: 17-Hydroxycorticosteroids; Adrenocorticotropic Hormone; Adult; Aged; Aldosterone; Angiotensin II; Di

1972
11-beta-hydrosylase deficiency: steroid response to sodium restriction and ACTH stimulation.
    The Journal of clinical endocrinology and metabolism, 1972, Volume: 35, Issue:2

    Topics: Adrenal Glands; Adrenal Hyperplasia, Congenital; Adrenocorticotropic Hormone; Aldosterone; Carbon Is

1972
Proceedings: Familial glucocorticoid deficiency.
    The Journal of endocrinology, 1974, Volume: 63, Issue:2

    Topics: 17-Hydroxycorticosteroids; Adrenocorticotropic Hormone; Adult; Aldosterone; Corticosterone; Cortison

1974
Plasma aldosterone in essential hypertension with low renin activity.
    Japanese circulation journal, 1974, Volume: 38, Issue:12

    Topics: Aldosterone; Body Weight; Corticosterone; Cushing Syndrome; Furosemide; Humans; Hydrochlorothiazide;

1974
17-Alpha-hydroxylase deficiency of the gonads and adrenals in a male pseudohermaphrodite.
    Acta endocrinologica. Supplementum, 1973, Volume: 173

    Topics: Adolescent; Adrenal Cortex Hormones; Adrenal Glands; Aldosterone; Corticosterone; Culture Techniques

1973
Isolated hypoaldosteronism.
    California medicine, 1973, Volume: 118, Issue:6

    Topics: Age Factors; Aged; Aldosterone; Humans; Male; Metabolism, Inborn Errors

1973
Primary amenorrhoea with hypertension due to 17-hydroxylase deficiency. Therapy with dexamethasone and ethinyloestradiol.
    Acta medica Scandinavica, 1973, Volume: 193, Issue:6

    Topics: Adult; Aldosterone; Amenorrhea; Dexamethasone; Diet, Sodium-Restricted; Estrogens; Ethinyl Estradiol

1973
Disturbance of cortisol production in congenital aldosterone deficiency.
    The Journal of clinical endocrinology and metabolism, 1972, Volume: 35, Issue:4

    Topics: Acetates; Aldosterone; Child Development; Child, Preschool; Desoxycorticosterone; Dexamethasone; Hum

1972
Hyperkalemia and renin deficiency.
    The New England journal of medicine, 1972, Sep-21, Volume: 287, Issue:12

    Topics: Aldosterone; Humans; Hyperkalemia; Kidney Diseases; Metabolism, Inborn Errors; Potassium; Renin; Sod

1972
A study of the renin-aldosterone system in congenital adrenal hyperplasia.
    The Journal of pediatrics, 1972, Volume: 81, Issue:5

    Topics: 17-Hydroxycorticosteroids; 17-Ketosteroids; Adrenal Hyperplasia, Congenital; Aldosterone; Blood Pres

1972
[Desoxycorticosterone hypersecretion and 18-hydroxy-DOC hypersecretion].
    Nihon rinsho. Japanese journal of clinical medicine, 1971, Volume: 29, Issue:3

    Topics: Adrenocortical Hyperfunction; Aldosterone; Cushing Syndrome; Desoxycorticosterone; Humans; Metabolis

1971
"Sephadex" column chromatography as an adjunct to competitive protein binding assays of steroids.
    Nature: New biology, 1971, Jul-07, Volume: 232, Issue:27

    Topics: Adrenal Cortex Hormones; Adrenal Gland Diseases; Aldosterone; Androgens; Androstanes; Androsterone;

1971
Exchangeable sodium and aldosterone secretion in children with congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
    Pediatric research, 1970, Volume: 4, Issue:2

    Topics: Adolescent; Adrenal Hyperplasia, Congenital; Adrenocortical Hyperfunction; Aldosterone; Child; Child

1970
Corticosteroid therapy in the neonatal period.
    Pediatric clinics of North America, 1970, Volume: 17, Issue:4

    Topics: Adrenal Gland Diseases; Adrenal Hyperplasia, Congenital; Adrenal Insufficiency; Aldosterone; Communi

1970
[Familial congenital hypoaldosteronism caused by 18-OH-dehydrogenase deficiency].
    Pediatric research, 1968, Volume: 2, Issue:6

    Topics: Adrenal Insufficiency; Aldosterone; Child; Child, Preschool; Corticosterone; Diet Therapy; Female; H

1968
Selective aldosterone deficiency.
    The Journal of clinical endocrinology and metabolism, 1969, Volume: 29, Issue:2

    Topics: 17-Ketosteroids; Adolescent; Adrenal Insufficiency; Aged; Aldosterone; Aminohippuric Acids; Carbon I

1969
Inborn errors in cortisol and aldosterone biosynthesis.
    The Journal of the Florida Medical Association, 1969, Volume: 56, Issue:4

    Topics: Adrenal Gland Diseases; Aldosterone; Humans; Hydrocortisone; Metabolism, Inborn Errors

1969