Hyper-IgD Syndrome / Hyperimmunoglobulinemia D With Recurrent Fever (HIDS) is a rare genetic disorder characterized by recurrent episodes of fever, abdominal pain, joint pain, and skin rashes. It is not contagious as it is caused by a mutation in the mevalonate kinase gene. HIDS is an autosomal recessive disorder, meaning it is inherited from both parents who are carriers of the gene mutation. It is important to consult with a healthcare professional for accurate diagnosis and management of this condition.
Hyper-IgD Syndrome / Hyperimmunoglobulinemia D With Recurrent Fever (HIDS) is a rare genetic disorder characterized by recurrent episodes of fever, accompanied by various symptoms such as abdominal pain, joint pain, and skin rashes. It is caused by mutations in the mevalonate kinase gene (MVK) and is inherited in an autosomal recessive manner.
Since HIDS is a genetic disorder, it is not contagious. It cannot be transmitted from person to person through direct contact, respiratory droplets, or any other means of transmission typically associated with contagious diseases.
The recurrent fevers in HIDS are triggered by various factors such as stress, infections, vaccinations, or exposure to certain medications. These fevers are a result of an overactive immune response and the excessive production of a protein called interleukin-1 beta.
While HIDS itself is not contagious, it is important to note that infections or illnesses that may trigger fever episodes in individuals with HIDS can be contagious. It is crucial for individuals with HIDS to take necessary precautions to avoid exposure to contagious diseases and maintain good hygiene practices.
It is recommended to consult with a healthcare professional or a genetic specialist for accurate diagnosis, management, and guidance regarding Hyper-IgD Syndrome / Hyperimmunoglobulinemia D With Recurrent Fever (HIDS).