Leptin Deficiency, also known as Congenital leptin deficiency (CLD), is a rare inherited disorder that causes early-onset obesity (in infants). Patients are born with normal weight, but they become...
What is Prader-Willi Syndrome?
Prader-Willi syndrome (PWS) is a rare multisystem genetic disorder affecting the metabolic, endocrine, and neurologic...
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...
Gigantism, also known as pediatric acromegaly and pituitary gigantism, is an extremely rare disorder in which a kid or adolescent has elevated quantities of...