iodine has been researched along with Tuberous Sclerosis in 3 studies
Iodine: A nonmetallic element of the halogen group that is represented by the atomic symbol I, atomic number 53, and atomic weight of 126.90. It is a nutritionally essential element, especially important in thyroid hormone synthesis. In solution, it has anti-infective properties and is used topically.
diiodine : Molecule comprising two covalently bonded iodine atoms with overall zero charge..
Tuberous Sclerosis: Autosomal dominant neurocutaneous syndrome classically characterized by MENTAL RETARDATION; EPILEPSY; and skin lesions (e.g., adenoma sebaceum and hypomelanotic macules). There is, however, considerable heterogeneity in the neurologic manifestations. It is also associated with cortical tuber and HAMARTOMAS formation throughout the body, especially the heart, kidneys, and eyes. Mutations in two loci TSC1 and TSC2 that encode hamartin and tuberin, respectively, are associated with the disease.
| Excerpt | Relevance | Reference |
|---|---|---|
| "One of the most interesting thing about tuberous sclerosis complex is the earliest skin manifestation represented by the hypomelanotic patches." | 1.42 | A different approach for identifying hypomelanotic macules in tuberous sclerosis complex. ( Boccardi, D; Gualandri, L; Menni, S, 2015) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (33.33) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (33.33) | 29.6817 |
| 2010's | 1 (33.33) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Gualandri, L | 1 |
| Boccardi, D | 1 |
| Menni, S | 1 |
| FANCONI, A | 1 |
| PRADER, A | 1 |
| ISLER, W | 1 |
| LUETHY, F | 1 |
| SIEBENMANN, R | 1 |
| Chudnow, RS | 1 |
| Wolfe, GI | 1 |
| Sparagana, SP | 1 |
| Delgado, MR | 1 |
| Batchelor, L | 1 |
| Roach, ES | 1 |
3 other studies available for iodine and Tuberous Sclerosis
| Article | Year |
|---|---|
A different approach for identifying hypomelanotic macules in tuberous sclerosis complex.
Topics: Adult; Child; Child, Preschool; Humans; Hypopigmentation; Sweat; Sweat Glands; Tuberous Sclerosis | 2015 |
[ADDISON'S DISEASE WITH CEREBRAL SCLEROSIS IN CHILDHOOD. A HEREDITARY SYNDROME TRANSMITTED THROUGH CHROMOSOME X?].
Topics: 17-Ketosteroids; Addison Disease; Adolescent; Adrenal Insufficiency; Adrenocorticotropic Hormone; Ch | 1963 |
Abnormal sudomotor function in the hypomelanotic macules of tuberous sclerosis complex.
Topics: Adolescent; Adult; Case-Control Studies; Child; Eccrine Glands; Female; Humans; Hypopigmentation; Io | 2000 |