Hypothyroidism causes
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Hypothyroidism Main page |
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
Causes
The most common cause of hypothyroidism is thyroiditis. Swelling and inflammation damage the thyroid gland's cells.
Causes of this problem include:
- The immune system attacking the thyroid gland
- Viral infections (common cold) or other respiratory infections
- Pregnancy (often called postpartum thyroiditis)
Other causes of hypothyroidism include:
- Certain medicines, such as lithium and amiodarone
- Congenital (birth) defects
- Radiation treatments to the neck or brain to treat different cancers
- Radioactive iodine used to treat an overactive thyroid gland
- Surgical removal of part or all of the thyroid gland
- Sheehan syndrome, a condition that may occur in a woman who bleeds severely during pregnancy or childbirth and causes the destruction of the pituitary gland
- Pituitary tumor or pituitary surgery
Life Threatening Causes
- Aneurysm
- Subarachnoid hemorrhage
- Craniopharyngioma
- Glioma
- Hypomelia
- Meningioma
- Metastasis
- Neoplastic
- Pituitary adenoma
- Pituitary apoplexy
- Pituitary cancer
- Syphilis
Common Causes
- Iodine deficiency
- Hashimoto's thyroiditis
- Thyroid hormone resistance
- Thyroid stimulating hormone deficiency
- Trh deficiency
- Tsh deficiency
Causes by Organ System
Causes in Alphabetical Order
- 17-beta-hydroxysteroid dehydrogenase iii deficiency
- Abnormal maternal iodine levels
- Acth deficiency
- Alström syndrome
- Aminoglutethimide
- Amiodarone
- Amyloidosis
- Aneurysm of the internal carotid artery
- Antithyroid drugs
- Anti-tsh receptor antibodies
- Apeced syndrome
- Atezolizumab
- Autoimmune disorders
- Autoimmune enteropathy
- Autoimmune polyendocrine syndrome type 3
- Autoimmune thyroiditis
- Axitinib
- Bamforth syndrome
- Bangstad syndrome
- Bexarotene
- Bilateral abductor vocal cord paralysis syndrome
- Brain-lung-thyroid syndrome
- Bromide
- Carbimazole
- Catch 22
- Cdg syndrome type 1a
- Central hypothyroidism
- 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
- 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
- Craniopharyngioma
- Cretinism athyreotic
- Cystinosis
- De quervain thyroiditis
- Deficiency of pit1
- Dermatosclerosis
- Diabetes insipidus
- Diabetes mellitus
- Diarrhea
- Digeorge syndrome
- Dopamine
- Down syndrome
- Ed-in-sol
- Emanuel syndrome
- Empty sella
- Enteropathy
- Escamilla-lisser syndrome
- Ethionamide
- Femiron
- Feosol
- Feostat
- Feratab
- Fer-gen-sol
- Fergon
- Fer-in-sol
- Ferrex
- Fibrous thyroiditis
- Glioma
- Goiter
- Graves disease
- Hashimoto's thyroiditis
- Hemochromatosis
- Hemocyte
- Hyperthyroidism
- Hypoadrenocorticism
- Hypomelia
- Hypopituitarism
- Hypothalamic dysfunction
- Hypothyroidism
- Hytinic
- Iatrogenic
- Icar
- Immune dysregulation
- Injury
- Interferon alfacon-1
- Interferon alpha
- Interferon-alfa
- Interleukin-2
- Iodine 131
- Iodine antenatal infection
- Iodine deficiency
- Iodine excess
- Ipex syndrome
- Ircon
- Iron overload
- Isolated tsh deficiency
- Johanson-blizzard syndrome
- Kaplowitz-bodurtha syndrome
- Kashin-bek disease
- Langerhans cell histiocytosis
- Lithium
- Lymphocytic hypophysitis
- Lymphocytic thyroiditis
- Lymphomatous thyroiditis
- Maternal antibody
- Meningioma
- Metastasis
- Methimazole
- Microcephaly
- Microphthalmia syndromic
- Mitotane
- Monosomy 1p36
- Multiple endocrine abnormalities
- Mutations
- Mycoses
- Neck radiotherapy
- Neck surgery
- Neonatal illness
- Neoplastic
- Nephro-fer
- Neurosarcoidosis
- Neutral lipid storage disease
- Niferex
- Nivolumab
- Nu-iron
- Obesity
- Ohdo syndrome
- Oxcarbazepine
- Panhypopituitarism
- Para-amino salicylic acid
- Pax8
- Peginterferon beta-1a
- Pegylated interferon alfa-2b
- Pembrolizumab
- Pendred's syndrome
- Perchlorate
- Pergolide
- Peripheral thyroid gland disorder resistance
- Phenytoin and levothyroxine interaction
- Pituitary adenoma
- Pituitary apoplexy
- Pituitary cancer
- Pituitary dwarfism type 3
- Pituitary dysfunction
- Poems syndrome
- Polyendocrinopathy
- Polyglandular disorders
- Postpartum thyroiditis
- Potassium iodide
- Pramipexole
- Previous grave's disease
- Primary hypothyroidism
- Propylthiouracil
- Pseudohypoparathyroidism type 1a
- Radiation therapy
- Radioactive iodine therapy
- Rathke's cleft cyst
- Reidel's thyroiditis
- Resistance to thyroid hormone
- Retinohepatoendocrinologic syndrome
- Rheumatoid arthritis
- Riedel syndrome
- Sarcoidosis
- Scleroderma
- Secondary hypothyroidism
- Septo-optic dysplasia
- Sheehan syndrome
- Silent thyroiditis
- Slow-fe
- Sorafenib
- Subacute granulomatous thyroiditis
- Subacute lymphocytic thyroiditis
- Subacute thyroiditis
- Subarachnoid hemorrhage
- Subtotal thyroidectomy
- Supprative thyroiditis
- Syphilis
- Thionamides
- Thyreostatic therapy
- Thyroid and cholestyramine interaction
- Thyroid dysgenesis
- Thyroid dyshormonogenesis
- Thyroid ectopy
- Thyroid hormone resistance
- Thyroid stimulating hormone deficiency
- Thyroidectomy
- Thyroiditis
- Tiagabine
- Tocilizumab
- Tositumomab iodine-131
- Trh deficiency
- Tsh deficiency
- Ttf-1
- Ttf-2
- Tuberculosis
- Turner syndrome
- Tyrosine kinase inhibitors
- Velocardiofacial syndrome
- Vilanova-canadeli syndrome
- Vitron-c
- Wolfram syndrome 2
- Zadik barak levin syndrome