Search results
Results from the WOW.Com Content Network
Cluster headache; Trigeminal nerve: Specialty: Neurology: Symptoms: Recurrent, severe headaches on one side of the head, eye watering, stuffy nose [1] Usual onset: 20 to 40 years old [2] Duration: 15 minutes to 3 hours [2] Types: Episodic, chronic [2] Causes: Unknown [2] Risk factors: Tobacco smoke, family history [2] Diagnostic method: Based ...
Needle-in-the-eye syndrome, sharp short-lived head pain, [1] jabs and jolts syndrome [2] Ophthalmodynia periodica , also known as " ice-pick headache ", is a primary headache disorder , so it is not caused by any other conditions.
Neurologists call headaches behind the eyes "retro-orbital headaches," which means "behind the eyeball socket." The rest of us call them "hell." The only thing worse than a headache is a headache ...
Symptoms include excruciating burning, stabbing, or electrical headaches mainly near the eye and typically these sensations are only on one side of the body. The headache attacks are typically accompanied by cranial autonomic signs that are unique to SUNCT. Each attack can last from five seconds to six minutes and may occur up to 200 times daily.
Drugmakers plan to raise U.S. prices on at least 250 branded medications including Pfizer COVID-19 treatment Paxlovid, Bristol Myers Squibb's cancer cell therapies and vaccines from France's ...
The diagnostic approach to headaches in children is similar to that of adults. However, young children may not be able to verbalize pain well. [83] If a young child is fussy, they may have a headache. [84] Approximately 1% of emergency department visits for children are for headache. [85] [86] Most of these headaches are not dangerous. The most ...
Certain medications can cause or worsen dry eyes, says Andreoli. These include diuretics, beta-blockers, antihistamines, decongestants, hormone replacement therapy, acne medication, and birth ...
Down syndrome or Down's syndrome, [12] also known as trisomy 21, is a genetic disorder caused by the presence of all or part of a third copy of chromosome 21. [3] It is usually associated with developmental delays, mild to moderate intellectual disability, and characteristic physical features.