Toxic multinodular goiter causes: Difference between revisions
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__NOTOC__ | __NOTOC__ | ||
{{Toxic multinodular goiter}} | {{Toxic multinodular goiter}} | ||
{{CMG}}; {{AE}} | {{CMG}}; {{AE}} {{SKA}} | ||
==Overview== | ==Overview== | ||
The progression to Toxic multinodular goiter usually involves the somatic gain-of-function mutations in the TSH receptor gene. | |||
==Causes== | ==Causes== | ||
The causes of toxic multinodular goiter are as follows:<ref name="urlDICER1 mutations in Familial Multi-Nodular Goiter with and without Ovarian Sertoli-Leydig Cell Tumors">{{cite web |url=https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3406486/ |title=DICER1 mutations in Familial Multi-Nodular Goiter with and without Ovarian Sertoli-Leydig Cell Tumors |format= |work= |accessdate=}}</ref><ref name="urlTSH-receptor autoantibodies - differentiation of hyperthyroidism between Graves disease and toxic multinodular goitre. - PubMed - NCBI">{{cite web |url=https://www.ncbi.nlm.nih.gov/pubmed/15127319 |title=TSH-receptor autoantibodies - differentiation of hyperthyroidism between Graves' disease and toxic multinodular goitre. - PubMed - NCBI |format= |work= |accessdate=}}</ref><ref name="urlHyperfunctioning thyroid nodules in toxic multinodular goiter share activating thyrotropin receptor mutations with solitary toxic adenoma. - PubMed - NCBI">{{cite web |url=https://www.ncbi.nlm.nih.gov/pubmed/9467563 |title=Hyperfunctioning thyroid nodules in toxic multinodular goiter share activating thyrotropin receptor mutations with solitary toxic adenoma. - PubMed - NCBI |format= |work= |accessdate=}}</ref><ref name="urlHyperfunctioning Thyroid Nodules in Toxic Multinodular Goiter Share Activating Thyrotropin Receptor Mutations with Solitary Toxic Adenoma1 | The Journal of Clinical Endocrinology & Metabolism | Oxford Academic">{{cite web |url=https://academic.oup.com/jcem/article/83/2/492/2865381/Hyperfunctioning-Thyroid-Nodules-in-Toxic |title=Hyperfunctioning Thyroid Nodules in Toxic Multinodular Goiter Share Activating Thyrotropin Receptor Mutations with Solitary Toxic Adenoma1 | The Journal of Clinical Endocrinology & Metabolism | Oxford Academic |format= |work= |accessdate=}}</ref> | |||
===Genetic Causes=== | ===Genetic Causes=== | ||
* | *The development of multi-nodular goiter is the result of multiple genetic base substitution mutations on exon 10 of chromosome 14q31. | ||
{| class="wikitable" | |||
!Frequency of mutation | |||
!TSHr gene codon | |||
!base substitution | |||
!amino acid change | |||
|- | |||
|'''Common''' | |||
|486 | |||
|ATC/ATG | |||
|Ile/Met | |||
|- | |||
|'''Common''' | |||
|632 | |||
|ACC/ATC | |||
|Thr/Ile | |||
|- | |||
|'''Less common''' | |||
|619 | |||
|GAT/GGT | |||
|Asp/Gly | |||
|- | |||
|'''Less common''' | |||
|623 | |||
|GCC/GTC | |||
|Ala/Val | |||
|- | |||
|'''Less common''' | |||
|629 | |||
|TTG/TTT | |||
|Leu/Phe | |||
|- | |||
|'''Less common''' | |||
|630 | |||
|ATC/CTC | |||
|Ile/Leu | |||
|- | |||
|'''Less common''' | |||
|633 | |||
|GAC/GAG | |||
|Asp/Glu | |||
|- | |||
|'''Less common''' | |||
|639 | |||
|CCA/TCA | |||
|Pro/Ser | |||
|} | |||
===Causes by Organ System=== | ===Causes by Organ System=== | ||
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|- bgcolor="LightSteelBlue" | |- bgcolor="LightSteelBlue" | ||
| '''Genetic''' | | '''Genetic''' | ||
| bgcolor="Beige" | | | bgcolor="Beige" | The development of multi-nodular goiter is the result of multiple genetic base substitution mutations on exon 10 of chromosome 14q31. | ||
|- | |- | ||
|- bgcolor="LightSteelBlue" | |- bgcolor="LightSteelBlue" | ||
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===Causes in Alphabetical Order=== | ===Causes in Alphabetical Order=== | ||
List the causes of the disease in alphabetical order. | List the causes of the disease in alphabetical order. | ||
{{columns-list | {{columns-list| | ||
* | * Genetic base substitution mutations on exon 10 of chromosome 14q31. | ||
* Cause 2 | * Cause 2 | ||
* Cause 3 | * Cause 3 |
Latest revision as of 23:08, 10 January 2020
Toxic multinodular goiter Microchapters |
Differentiating Toxic multinodular goiter from other Diseases |
---|
Diagnosis |
Treatment |
Case Studies |
Toxic multinodular goiter causes On the Web |
American Roentgen Ray Society Images of Toxic multinodular goiter causes |
Risk calculators and risk factors for Toxic multinodular goiter causes |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Sunny Kumar MD [2]
Overview
The progression to Toxic multinodular goiter usually involves the somatic gain-of-function mutations in the TSH receptor gene.
Causes
The causes of toxic multinodular goiter are as follows:[1][2][3][4]
Genetic Causes
- The development of multi-nodular goiter is the result of multiple genetic base substitution mutations on exon 10 of chromosome 14q31.
Frequency of mutation | TSHr gene codon | base substitution | amino acid change |
---|---|---|---|
Common | 486 | ATC/ATG | Ile/Met |
Common | 632 | ACC/ATC | Thr/Ile |
Less common | 619 | GAT/GGT | Asp/Gly |
Less common | 623 | GCC/GTC | Ala/Val |
Less common | 629 | TTG/TTT | Leu/Phe |
Less common | 630 | ATC/CTC | Ile/Leu |
Less common | 633 | GAC/GAG | Asp/Glu |
Less common | 639 | CCA/TCA | Pro/Ser |
Causes by Organ System
Cardiovascular | No underlying causes |
Chemical/Poisoning | No underlying causes |
Dental | No underlying causes |
Dermatologic | No underlying causes |
Drug Side Effect | No underlying causes |
Ear Nose Throat | No underlying causes |
Endocrine | No underlying causes |
Environmental | No underlying causes |
Gastroenterologic | No underlying causes |
Genetic | The development of multi-nodular goiter is the result of multiple genetic base substitution mutations on exon 10 of chromosome 14q31. |
Hematologic | No underlying causes |
Iatrogenic | No underlying causes |
Infectious Disease | No underlying causes |
Musculoskeletal/Orthopedic | No underlying causes |
Neurologic | No underlying causes |
Nutritional/Metabolic | No underlying causes |
Obstetric/Gynecologic | No underlying causes |
Oncologic | No underlying causes |
Ophthalmologic | No underlying causes |
Overdose/Toxicity | No underlying causes |
Psychiatric | No underlying causes |
Pulmonary | No underlying causes |
Renal/Electrolyte | No underlying causes |
Rheumatology/Immunology/Allergy | No underlying causes |
Sexual | No underlying causes |
Trauma | No underlying causes |
Urologic | No underlying causes |
Miscellaneous | No underlying causes |
Causes in Alphabetical Order
List the causes of the disease in alphabetical order.
- Genetic base substitution mutations on exon 10 of chromosome 14q31.
- Cause 2
- Cause 3
- Cause 4
- Cause 5
- Cause 6
- Cause 7
- Cause 8
- Cause 9
- Cause 10