|
|
Line 1: |
Line 1: |
| __NOTOC__ | | __NOTOC__ |
| {{Hypothyroidism}} | | {{Hypothyroidism}} |
| {{CMG}} {{AE}} | | {{CMG}} {{AE}} {{VP}} {{LRO}} |
|
| |
|
| ==Overview== | | ==Overview== |
| | | Hypothyroidism is commonly caused by [[iodine]] deficiency, [[hashimoto's thyroiditis]], and diseases that cause disruption in [[pituitary]] [[hormone]] production. [[Neoplasms]] can be a life threatening cause of hypothyroidism and require prompt diagnosis and differentiation to reduce morbidity. |
| ==Causes== | | ==Causes== |
| <div style="-webkit-user-select: none;"> | | <div style="-webkit-user-select: none;"> |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Associate Editor(s)-in-Chief: Vignesh Ponnusamy, M.B.B.S. [2] Luke Rusowicz-Orazem, B.S.
Overview
Hypothyroidism is commonly caused by iodine deficiency, hashimoto's thyroiditis, and diseases that cause disruption in pituitary hormone production. Neoplasms can be a life threatening cause of hypothyroidism and require prompt diagnosis and differentiation to reduce morbidity.
Causes
Life Threatening Causes
Common Causes
Less Common Causes
- Hypothyroidism can result from postpartum thyroiditis, a condition that affects about 5% of all women within a year after giving birth. The first phase is typically hyperthyroidism. Then, the thyroid either returns to normal or a woman develops hypothyroidism. Of those women who experience hypothyroidism associated with postpartum thyroiditis, one in five will develop permanent hypothyroidism requiring life-long treatment.
- Hypothyroidism can also result from sporadic inheritance, sometimes autosomal recessive.
Causes by Organ System
Cardiovascular
|
Alström syndrome, Aneurysm of the internal carotid artery, Neutral lipid storage disease
|
Chemical/Poisoning
|
Iodine 131, Iodine antenatal infection , Iron overload , Isolated tsh deficiency, Lithium, Potassium iodide
|
Dental
|
No underlying causes
|
Dermatologic
|
Dermatosclerosis
|
Drug Side Effect
|
Aminoglutethimide, Amiodarone, Antithyroid drugs, Atezolizumab, Axitinib, Bexarotene, Bromide , Carbimazole, Catch 22 , Ed-in-sol, Ethionamide, Femiron, Feosol, Feostat, Feratab, Fer-gen-sol, Fergon, Fer-in-sol, Ferrex, Hytinic, Icar, Interferon alfacon-1, Interferon alpha, Interferon-alfa, Interleukin-2, Ircon, Methimazole, Mitotane, Nephro-fer, Niferex, Nivolumab, Nu-iron, Oxcarbazepine, Para-amino salicylic acid, Peginterferon beta-1a, Pegylated interferon alfa-2b, Pembrolizumab, Perchlorate, Pergolide, Phenytoin and levothyroxine interaction, Pramipexole, Propylthiouracil, Slow-fe, Sorafenib, Thionamides, Thyroid and cholestyramine interaction, Tiagabine, Tocilizumab, Tositumomab iodine-131, Ttf-1, Ttf-2, Tyrosine kinase inhibitors, Vitron-c
|
Ear Nose Throat
|
Bilateral abductor vocal cord paralysis syndrome
|
Endocrine
|
Abnormal maternal iodine levels, Acth deficiency, Antithyroid drugs, Apeced syndrome, Autoimmune polyendocrine syndrome type 3, Autoimmune thyroiditis, Brain-lung-thyroid syndrome, Central hypothyroidism, Chronic autoimmune thyroiditis, Combined pituitary hormone deficiency 1 (pou1f1 gene), Combined pituitary hormone deficiency 2 (prop1 gene), Combined pituitary hormone deficiency 3 (lhx gene), Congenital disorder of glycosylation type 1a , Congenital disorder of glycosylation type 1h , Congenital thyroid dysgenesis, Cretinism athyreotic , De quervain thyroiditis, Deficiency of pit1, Dopamine, Empty sella, Escamilla-lisser syndrome , Fibrous thyroiditis, Goiter , Graves disease , Hashimoto's thyroiditis, Hemochromatosis, Hyperthyroidism , Hypoadrenocorticism , Hypomelia , Hypopituitarism, Hypothalamic dysfunction , Hypothyroidism, Iodine deficiency, Iodine excess, Kaplowitz-bodurtha syndrome , Lymphocytic hypophysitis, Lymphocytic thyroiditis, Lymphomatous thyroiditis , Multiple endocrine abnormalities , Panhypopituitarism, Peripheral thyroid gland disorder resistance, Pituitary adenoma, Pituitary apoplexy, Pituitary cancer , Pituitary dwarfism type 3, Pituitary dysfunction , Polyendocrinopathy, Polyglandular disorders, Postpartum thyroiditis , Primary hypothyroidism, Pseudohypoparathyroidism type 1a, Rathke's cleft cyst, Reidel's thyroiditis, Resistance to thyroid hormone , Retinohepatoendocrinologic syndrome , Riedel syndrome , Secondary hypothyroidism, Sheehan syndrome, Silent thyroiditis, Subacute granulomatous thyroiditis, Subacute lymphocytic thyroiditis, Subacute thyroiditis, Subtotal thyroidectomy, Supprative thyroiditis, Thyreostatic therapy, Thyroid dysgenesis , Thyroid dyshormonogenesis , Thyroid ectopy, Thyroid hormone resistance , Thyroid stimulating hormone deficiency, Thyroidectomy, Thyroiditis, Trh deficiency, Tsh deficiency
|
Environmental
|
No underlying causes
|
Gastroenterologic
|
Diarrhea, Enteropathy, Retinohepatoendocrinologic syndrome
|
Genetic
|
17-beta-hydroxysteroid dehydrogenase iii deficiency , Abnormal maternal iodine levels, Acth deficiency, Alström syndrome, Bamforth syndrome , Bangstad syndrome , Cdg syndrome type 1a , Chromosome 1, 1p36 deletion syndrome , Chromosome 10, monosomy 10p , Chromosome 10p deletion syndrome, Chromosome 12 ring syndrome , Chromosome 15q duplication syndrome , Chromosome 15q, trisomy , Chromosome 2 trisomy syndrome , Chromosome 6, trisomy 6q , Chromosome 6q duplication syndrome , Combined pituitary hormone deficiency 1 (pou1f1 gene), Combined pituitary hormone deficiency 2 (prop1 gene), Combined pituitary hormone deficiency 3 (lhx gene), Congenital disorder of glycosylation type 1a , Congenital disorder of glycosylation type 1h , Congenital thyroid dysgenesis, Cystinosis, Deficiency of pit1, Digeorge syndrome, Down syndrome, Emanuel syndrome, Ipex syndrome, Johanson-blizzard syndrome , Kaplowitz-bodurtha syndrome , Langerhans cell histiocytosis, Monosomy 1p36 , Mutations , Ohdo syndrome, Pax8, Pendred's syndrome , Poems syndrome, Septo-optic dysplasia, Turner syndrome, Velocardiofacial syndrome , Vilanova-canadeli syndrome , Wolfram syndrome 2 , Zadik barak levin syndrome
|
Hematologic
|
Diabetes insipidus, Diabetes mellitus, Hemochromatosis, Hemocyte, Iodine deficiency, Iodine excess, Iron overload , Isolated tsh deficiency, Maternal antibody, Subarachnoid hemorrhage
|
Iatrogenic
|
Iatrogenic, Neck radiotherapy, Neck surgery, Radiation therapy, Radioactive iodine therapy, Subtotal thyroidectomy, Supprative thyroiditis, Thyroidectomy
|
Infectious Disease
|
Iodine antenatal infection , Mycoses, Rathke's cleft cyst, Syphilis, Tuberculosis
|
Musculoskeletal/Orthopedic
|
Bilateral abductor vocal cord paralysis syndrome
|
Neurologic
|
Aneurysm of the internal carotid artery, Brain-lung-thyroid syndrome, Craniopharyngioma, Dopamine, Down syndrome, Microcephaly , Microphthalmia syndromic, Neurosarcoidosis , Subarachnoid hemorrhage
|
Nutritional/Metabolic
|
Diabetes insipidus, Diabetes mellitus, Diarrhea, Obesity
|
Obstetric/Gynecologic
|
Neonatal illness, Sheehan syndrome
|
Oncologic
|
Craniopharyngioma, Glioma, Hypomelia , Meningioma, Metastasis, Neoplastic, Pituitary adenoma, Pituitary apoplexy, Pituitary cancer
|
Ophthalmologic
|
No underlying causes
|
Overdose/Toxicity
|
No underlying causes
|
Psychiatric
|
No underlying causes
|
Pulmonary
|
Amyloidosis, Tuberculosis
|
Renal/Electrolyte
|
No underlying causes
|
Rheumatology/Immunology/Allergy
|
Amyloidosis, Anti-tsh receptor antibodies, Apeced syndrome, Autoimmune disorders, Autoimmune enteropathy, Autoimmune polyendocrine syndrome type 3, Autoimmune thyroiditis, Chronic autoimmune thyroiditis, Dermatosclerosis, Fibrous thyroiditis, Graves disease , Immune dysregulation , Kashin-bek disease , Langerhans cell histiocytosis, Neurosarcoidosis , Rheumatoid arthritis, Sarcoidosis, Scleroderma
|
Sexual
|
Syphilis
|
Trauma
|
Injury
|
Urologic
|
No underlying causes
|
Miscellaneous
|
No underlying causes
|
Causes in Alphabetical Order
The unnamed parameter 2= is no longer supported. Please see the documentation for {{
columns-list}}.
3
References
Template:WS
Template:WH