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Early eponym use: was gradually replaced by Hodgkin’s disease in the first quarter of the 20th century. Hecker’s disease is a rare form of generalized osteoporosis and Paget’s disease.
Chronic disorders of the exocrine pancreas, such as chronic pancreatitis and diabetes mellitus have contributed their names to the disease in the 20th century.
Growth disturbances that are not associated with aging, like familial gigantism, are included under the name.
It is classified as an Adzuki disease in Japan, Acrofacial dysostosis (AFD) in Australia and New Zealand, Acquired hypoglycemia of childhood (AHC), growth retardation, linear growth failure (LRF) in Southern India, acanthosis nigricans, Leopard syndrome, tricho-rhino-phalangeal syndrome (TRPS), and Warted Hand Syndrome (WHS) in the United States and Europe. It is commonly used as a synonym for Growth hormone deficiency (GHD) in the Western world.
It is characterized in most affected individuals by growth failure, with abnormal facial features, skeletal abnormalities, and endocrinopathies. In some cases of growth failure, it is difficult to distinguish it from AHC, and people with different characteristics, especially in the presence of skeletal abnormalities, have been described as having different genotypes, differing in prevalence between populations. This forms the basis of the concept that the two disorders are not the same.
The term “Kawasaki syndrome” was first introduced in 1966 by Dr. M. Kawasaki.
Kawasaki syndrome was originally classified into