Related Experiment Video
Updated: May 2, 2026

11:02
Isolation and Physiological Analysis of Mouse Cardiomyocytes
Published on: September 7, 2014
22.9K
[Cardiac myopathy due to overt hypothyroidism]
B Harbeck1, M J Berndt1, H Lehnert1
1Medizinische Klinik 1, Universitätsklinikum Schleswig-Holstein Campus Lübeck.
Deutsche Medizinische Wochenschrift (1946)
|February 27, 2014
Summary
Severe hypothyroidism can manifest as muscle weakness and cardiac issues. Prompt treatment with levothyroxine can lead to recovery.
Area of Science:
- Endocrinology
- Cardiology
- Neurology
Background:
- Hypothyroidism is a common endocrine disorder.
- Severe hypothyroidism can lead to various systemic complications.
- Myopathy and cardiac involvement are less common presentations.
Observation:
- A 51-year-old male presented with fatigue, proximal muscle weakness, hair loss, and weight gain.
- Physical examination revealed pretibial myxedema and dry skin.
- Laboratory tests showed elevated cardiac enzymes and marked hypothyroidism.
Findings:
- Investigations including ECG, echocardiography, and imaging were normal.
- Thyroid ultrasound indicated Hashimoto thyroiditis.
- Diagnosis of overt hypothyroidism with myxedema and rhabdomyolysis was confirmed.
Implications:
- This case highlights that severe overt hypothyroidism can present primarily as myopathy with myositis and cardiac involvement.
- Early diagnosis and treatment are crucial for managing hypothyroidism-related complications.
- Further research may explore the mechanisms linking hypothyroidism to myopathy and cardiac dysfunction.
Related Concept Videos
Hyperthyroidism II: Pathophysiology
28
Hyperthyroidism is a hypermetabolic state caused by elevated levels of thyroid hormones, triiodothyronine (T3) and thyroxine (T4). It results from dysregulation at the thyroid, pituitary, or immune system level and affects multiple organ systems.PathophysiologyThe most common cause of hyperthyroidism is Graves’ disease, an autoimmune disorder in which antibodies, specifically thyroid-stimulating antibodies (TSAb), a subtype of TSH receptor antibodies (TRAb), bind to and activate TSH...
28
Hypothyroidism II: Pathophysiology
26
Hypothyroidism is a disorder characterized by insufficient production of thyroid hormones, which regulate metabolism, energy balance, and multiple organ systems.TypesHypothyroidism is classified based on the level of dysfunction. Primary hypothyroidism results from intrinsic thyroid gland dysfunction, causing reduced hormone production despite normal or increased stimulation. Secondary hypothyroidism arises from inadequate thyroid-stimulating hormone (TSH) secretion by the pituitary. Tertiary...
26
Hyperthyroidism I: Introduction
30
Hyperthyroidism is a type of thyrotoxicosis characterized by the thyroid gland's overproduction of the thyroid hormones triiodothyronine (T3) and thyroxine (T4). This hormone excess increases the basal metabolic rate and enhances sensitivity to catecholamines.DiagnosisDiagnosis is based on clinical features and biochemical testing. It typically shows suppressed thyroid-stimulating hormone (TSH) levels below 0.4 mIU/L, with elevated free T3 and/or T4. Additional tests, including thyroid...
30
Graves' Disease I: Introduction
23
Graves' disease is an autoimmune disorder that causes hyperthyroidism, or overactivity of the thyroid gland. It results from autoantibodies called thyroid-stimulating immunoglobulins (TSIs), which bind to thyroid-stimulating hormone (TSH) receptors, leading to overstimulation of hormone production and a hypermetabolic state.EtiologyAlthough considered idiopathic, Graves’ disease has well-established contributing factors. There is a strong genetic component, with increased prevalence...
23
Graves Disease II: Pathophysiology
26
Graves’ disease is an autoimmune disorder characterized by the production of thyroid-stimulating immunoglobulins (TSI) that activate TSH receptors, leading to excessive synthesis and release of thyroid hormones (T3 and T4) and resulting in hyperthyroidism.Among all causes of hyperthyroidism, Graves’ disease is the most common and can happen at any age, though it is more frequent in women. It produces a hypermetabolic state with features such as weight loss, tachycardia, tremor,...
26
Cardiomyopathy III: Hypertrophic Cardiomyopathy
805
Hypertrophic cardiomyopathy, or HCM, is an autosomal dominant genetic disorder characterized by asymmetric left ventricular hypertrophy without ventricular dilation. It is more common in men and is typically diagnosed in young, athletic adults.EtiologyHCM is primarily genetic and is caused by mutations in genes encoding sarcomeric proteins. Researchers have identified over 1400 mutations across at least 11 different genes. Among these, the most frequently occurring mutations are found in the...
805

