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hypohidrosis/febbre
Il collegamento viene salvato negli appunti
Pagina 1 a partire dal 135 risultati
Topiramate associated hypohidrosis and hyperthermia.
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Topiramate is a new antiepileptic drug, used for treatment of partial onset seizure and refractory seizures. Although it is well tolerated in children, some adverse effects including hypohidrosis and hyperthermia are reported. We present two children with epilepsy who were treated with topiramate
Hypohidrosis and hyperthermia during topiramate treatment in children.
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Topiramate is one of the newer generation antiepileptic drugs with a beneficial clinical effect on various seizure types. In this study, we present the clinical findings of hypohidrosis and hyperthermia with topiramate in pediatric patients. The data were collected retrospectively on 173 patients
[Anhidrosis and hyperthermia associated with treatment with topiramate].
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BACKGROUND
It has been observed that if topiramate (TPM) is given together with other antiepileptic drugs when the temperature of the environment is high, a disorder involving sweating and thermo regulation may be seen as a side effect.
METHODS
We describe ten patients, of an average age of 7 years
Case records of the Massachusetts General Hospital. Weekly clinicopathological exercises. Case 29-1994. A 32-year-old man with exercise-induced hyperthermia and acquired anhidrosis.
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Anhidrosis manifesting as low grade pyrexia (cas report).
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Bilateral Adie's tonic pupil with anhidrosis and hyperthermia.
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A Case Report of Congenital Insensitivity to Pain and Anhidrosis (CIPA).
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Congenital insensitivity to pain and anhidrosis (CIPA) or hereditary sensory autonomic neuropathies type IV (HSAN type IV) is an extremely rare autosomal recessive disorder initially described by Swanson in 1963. We report a 2.5-year-old boy with clinical features of CIPA as the first case in Iran.
Phenotypic and genotypic features of a pair of Chinese identical twins with congenital insensitivity to pain and anhidrosis: A case report.
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BACKGROUND
Congenital insensitivity to pain with anhidrosis (CIPA) is a rare autosomal recessive genetic disorder characterized by insensitivity to noxious stimulus and the absence of sweating. Fractures and joint destruction are common complications, but detailed studies on mineral and skeletal
Hypohidrosis-related symptoms in pediatric epileptic patients with topiramate.
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BACKGROUND
Topiramate is one of the most commonly prescribed newer antiepileptic drugs. However, we have encountered quite a few cases of pediatric epileptic patients on topiramate complaining about the symptoms related to hypohidrosis. The aim of this study was to determine the incidence and define
Congenital insensitivity to pain with anhidrosis: a case report of a 33-year-old patient.
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Congenital insensitivity to pain with anhidrosis is a type IV hereditary sensory and autonomic neuropathy, presenting early in life. This disorder results from defective neural crest differentiation with loss of the first-order afferent system, which is responsible for sensations of pain and
Catastrophic results due to unrecognizing of congenital insensitivity to pain with anhidrosis in children with multiple long bones fractures: A case report of 27 years follow-up of two siblings
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Introduction: Congenital insensitivity to pain with anhidrosis (CIPA; OMIM 256,800) is a rare autosomal recessive disease. Although the clinical symptoms are known, the consensus of CIPA treatment has not been recognized. This is the
Anesthetic management during adenotonsillectomy for twins with congenital insensitivity to pain with anhidrosis: two case reports.
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BACKGROUND
Congenital insensitivity to pain with anhidrosis is a rare autosomal recessive disorder characterized by hyperpyrexia, anhidrosis, pain insensitivity, self-inflicted injuries, and intellectual disability. The anesthetic management of these patients is challenging owing to the high risk of
[Congenital insensitivity to pain with anhidrosis associated with congenital myasthenic syndrome].
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BACKGROUND
Congenital insensitivity to pain with anhidrosis (CIPA) or hereditary sensory and autonomic neuropathy type IV (HSAN IV) is a rare autosomal recessive disorder featuring recurrent fever episodes, inability to sweat, absent response to noxious stimuli, self mutilating behavior and mental
Epidural anesthesia and the thermoregulatory responses to hyperthermia--preliminary observations in volunteer subjects.
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BACKGROUND
Clinical reports associate the use of epidural anesthesia with an increase in core temperature in women in labor. We tested the hypothesis that epidural anesthesia alters thermoregulatory responses to hyperthermia in human volunteers.
METHODS
Each of four volunteers were studied on two
Post-typhoid anhidrosis: a clinical curiosity.
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A 19-year-old girl developed generalised anhidrosis following typhoid fever. Elaborate investigations disclosed nothing abnormal. A skin biopsy revealed the presence of atrophic as well as normal eccrine glands. This appears to be the third case of its kind in the English literature. It is
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