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hypohidrosis/headache

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Raeder's syndrome: "anhidrosis", headache, and a proposal for a new classification.

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Identifikohuni Regjistrohu

Symptomatic cluster headache in internal carotid artery dissection--consider anhidrosis.

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Raeder's Paratrigeminal Syndrome: Headache and Horner's Lacking Anhidrosis.

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Hypohidrosis during topiramate treatment: a rare and reversible side effect.

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Identifikohuni Regjistrohu
Topiramate is an antiepileptic drug with a beneficial clinical effect on various seizure types. Topiramate does not seem to be associated with serious adverse effects and is also well tolerated in pediatric patients. Only few cases of hypohidrosis have been described. This report presents one young

[Progression of cluster headache to Raeder's syndrome with marked response to corticosteroid therapy: a case report].

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Identifikohuni Regjistrohu
A 42-year-old man complained of severe left orbital pain for 7 months. The diagnosis of cluster headache was made on the basis of diagnostic criteria formed by the International Headache Society. Sumatriptan was effective in relieving pain to a certain degree, but the frequency of the occurrence of

Subcutaneous sumatriptan in cluster headache: a time study of the effect on pain and autonomic symptoms.

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Identifikohuni Regjistrohu
A subcutaneous injection of 6 mg sumatriptan rapidly and effectively stopped attacks of cluster headache. After a time lag of 4-14 minutes (mean 7 minutes) pain dramatically dropped to zero within seconds to single minutes (mean 56 seconds). This rapid effect may indicate that mere vasoconstriction

Chronic paroxysmal hemicrania: from the index patient to the disease.

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The first patient with chronic paroxysmal hemicrania (CPH), a 41-year-old woman, first seen in 1961, was followed until an adequate treatment was found, 12 years later. Clinically, attack frequency and duration differed widely from the general pattern of cluster headache. Ocular variables, such as

[The effect of a water-cooled vest on heat intolerance in a patient with anhidrosis due to familial amyloidosis of Finnish type].

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Identifikohuni Regjistrohu
The patient was a 70-year-old male with familial amyloidosis of Finnish type who complained of heat intolerance due to anhidrosis during outdoor activities in summer. A water-cooled TM-2 vest was tried for this patient to reduce his body heat during exercises. Following the morning activities

Exercise as disease detector.

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Identifikohuni Regjistrohu
Exercise is a well-known stress test for uncovering heart or lung disease, but it can also stress other organs and unmask a range of medical disorders. Practical case examples are given in seven areas: anemia, headache, hematuria, gastrointestinal problems, seizure, anhidrosis, and hypothyroidism.

Agenesis of the internal carotid artery associated with ipsilateral Horner syndrome in a child.

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Identifikohuni Regjistrohu
Agenesis of the internal carotid artery is a rare, usually asymptomatic congenital anomaly. Patients may remain asymptomatic because a network of collaterals develops in response to agenesis of the internal carotid artery, which is usually diagnosed as an incidental finding after magnetic resonance

Naphazoline as a confounder in the diagnosis of carotid artery dissection.

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Identifikohuni Regjistrohu
Diagnosing Horner Syndrome can be difficult in the setting of an incomplete triad. A 27-year-old man presented with unilateral eyelid droop and intermittent ipsilateral headaches, having already seen 7 physicians. Physical examination revealed unilateral ptosis but no pupillary miosis or facial

[Spontaneous dissection of the internal carotid artery. Apropos of 7 cases and a review of the literature].

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Identifikohuni Regjistrohu
Since 1978, the authors have observed 7 cases of dissecting aneurysm in the internal carotid artery. Symptoms were severe headache and subsequent neurologic deficit in young persons (3 women, 4 men; mean age 35 years). The underlying pathology was spontaneous dissection of the cervical internal

Fabry disease in children: agalsidase-beta enzyme replacement therapy.

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Identifikohuni Regjistrohu
Fabry disease is a rare, multiorgan disease. The most serious complications involve the kidney, brain and heart. This study aims to assess the effect of enzyme replacement therapy (ERT) using agalsidase-beta in children with Fabry disease. We carried out a nationwide, descriptive and observational

Isolated Horner syndrome as a rare initial presentation of nasopharyngeal carcinoma: a case report.

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Identifikohuni Regjistrohu
UNASSIGNED Horner syndrome refers to a set of clinical presentations resulting from disruption of sympathetic innervation to the eye and adnexa. Classically, the clinical triad consists of ipsilateral blepharoptosis, pupillary miosis, and facial anhidrosis. Ocular sympathetic denervation may signify

Topical glycopyrrolate for patients with facial hyperhidrosis.

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Identifikohuni Regjistrohu
BACKGROUND Facial hyperhidrosis may negatively impact the quality of life. Although various conservative modalities have been suggested, the condition is not often treated successfully. OBJECTIVE To examine whether topical glycopyrrolate could be an effective and safe treatment for facial
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