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Weird Health News

Sleeping Beauty Syndrome

Sleeping Beauty Syndrome

Kleine-Levin Syndrome is a rare sleep disorder characterized by episodes of excessive sleepiness, behavioral changes, and cognitive symptoms. While the cause of KLS is not fully understood, it is thought to be related to a dysfunction in the hypothalamus. Treatment primarily involves managing the symptoms during episodes, and the outlook for individuals with KLS is generally good, although some individuals may continue to experience episodes throughout their lifetime. If you or a loved one are experiencing symptoms of KLS, it is important to speak with a healthcare provider for proper diagnosis and treatment.
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Acromegaly

Acromegaly

Acromegaly is a rare hormonal disorder characterized by excessive growth hormone production in adults. Its signs and symptoms gradually develop over time, affecting various body parts and leading to metabolic changes. The primary cause is a benign tumor in the pituitary gland. Early diagnosis, through physical examination, laboratory tests, and imaging, is crucial for effective management. Treatment options include surgery, medications, and radiation therapy, tailored to the individual's needs. With appropriate care, individuals with acromegaly can lead fulfilling lives. If you suspect you or someone you know may have acromegaly, seek medical attention promptly for a comprehensive evaluation.
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Foreign Body Granuloma

Foreign Body Granuloma

Foreign Body Granuloma is an inflammatory response that occurs when the body reacts to the presence of a foreign object or substance. It manifests as a localized swelling, redness, and pain. The condition can be caused by various foreign objects entering the body. Diagnosis involves a physical examination and diagnostic tests. Treatment usually involves surgical removal or drainage of the granuloma, leading to resolution and healing. The outlook is generally positive, but complications can occur in rare cases.
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Congenital Insensitivity to Pain

Congenital Insensitivity to Pain

Congenital Insensitivity to Pain is a rare genetic disorder characterized by the inability to feel physical pain. While its history can be traced back to the early 1930s, our understanding of the condition has grown through genetic research. Its signs and symptoms include the lack of pain sensitivity and, in some cases, reduced sensitivity to temperature and touch. CIP is caused by mutations in the SCN9A gene, affecting the transmission of pain signals in the nervous system. Diagnosis involves a combination of family history, clinical examination, and genetic testing. Although there is no cure, early intervention and careful monitoring can help manage the condition and prevent complications. The outlook for those with CIP is dependent on proper management and support. Living without pain may seem intriguing, but it's essential to recognize the risks associated with the absence of this protective mechanism. With vigilant care and attention, individuals with CIP can lead fulfilling lives despite the challenges posed by this rare disorder.
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