Hunter Syndrome: Understanding This Rare Genetic Disorder
Hunter syndrome (also known as mucopolysaccharidosis II or MPS II) is a rare X-linked recessive lysosomal storage disorder with a significantly higher prevalence in...
Pseudohypoparathyroidism: Decoding the Rare Disorder
Pseudohypoparathyroidism (PHP) is a rare hereditary disorder characterized by the resistance or insensitivity of target organs to parathyroid hormone (PTH). The parathyroid glands are...
Prader-Willi Syndrome: Understanding the Genetic Disorder
What is Prader-Willi Syndrome?
Prader-Willi syndrome (PWS) is a rare multisystem genetic disorder affecting the metabolic, endocrine, and neurologic systems due to abnormalities on chromosome...
Graves Eye Disease: Symptoms, Risks & Treatment Options
Graves' Eye Disease, also known as Graves' ophthalmopathy or thyroid eye disease (TED), is an autoimmune disorder characterized by inflammation and swelling of the...
Thyrotoxic Crisis: Understanding the Signs, Causes & Treatment
Also known as a thyroid storm, thyrotoxic crisis is an emergency condition caused by excessively high levels of thyroid hormone in the blood. This...
Hashimoto’s Thyroiditis: Exploring Symptoms and Solutions
Hashimoto's Thyroiditis, also known as autoimmune thyroiditis or chronic lymphocytic thyroiditis, is a condition in which the immune system attacks the thyroid gland, leading...
