The ICD-10 code for Leprechaunism is E74.8. However, there is no specific ICD-9 code for Leprechaunism as it is a rare genetic disorder. Leprechaunism, also known as Donohue syndrome, is an extremely rare and severe form of insulin resistance. It is characterized by growth delays, facial abnormalities, and other physical and developmental issues. Proper medical diagnosis and management are crucial for individuals with this condition.
Leprechaunism, also known as Donohue syndrome, is an extremely rare genetic disorder characterized by severe insulin resistance. It is named after the mythical Irish creatures known as leprechauns due to the characteristic facial features of affected individuals. The ICD-10 code for Leprechaunism is E13.8, which falls under the category of "Other specified diabetes mellitus."
In contrast, the ICD-9 code for Leprechaunism is 277.89, categorized as "Other specified disorders of metabolism." However, it is important to note that the ICD-9 code system was replaced by ICD-10 in October 2015, as it provides more detailed and specific codes for various conditions.
Leprechaunism is an autosomal recessive disorder caused by mutations in the insulin receptor gene (INSR). These mutations impair the normal functioning of the insulin receptor, leading to severe insulin resistance. As a result, affected individuals experience high levels of glucose in their blood, leading to various health complications.
Symptoms of Leprechaunism include growth retardation, hypertrichosis (excessive hair growth), characteristic facial features, enlarged genitals, and other metabolic abnormalities. The disorder is typically diagnosed in infancy or early childhood based on clinical features, hormone levels, and genetic testing.
Due to its rarity, treatment options for Leprechaunism are limited, and management mainly focuses on controlling blood sugar levels and addressing associated health issues. Close monitoring by a multidisciplinary medical team is essential to ensure the best possible outcomes for affected individuals.