Long-term follow-up in pediatric patients with paroxysmal hypothermia (Shapiro's syndrome).
Eur J Paediatr Neurol
; 22(6): 1081-1086, 2018 Nov.
Article
em En
| MEDLINE
| ID: mdl-30195408
ABSTRACT
INTRODUCTION:
Shapiro syndrome (SS) is characterized by spontaneous recurrent episodes of hypothermia, hyperhidrosis and corpus callosum (CC) agenesis. Less than 60 cases have been reported to date and the pathogenic mechanism as well as the prognosis of this syndrome are still debated. We describe the clinical features and long-term follow-up of a pediatric cohort of SS patients.METHODS:
We collected 13 (10 novel) pediatric cases of SS and report their long-term follow-up and neurological outcome.RESULTS:
All patients experienced recurring hypothermia, with body temperature below 35 °C during the episodes, often accompanied by hyperidrosis. CC agenesis was an inconstant structural feature in the present series (2/13 patients). Seven patients received antiepileptic drugs (AEDs) or other drug therapy for a mean period of 12 months. At long-term follow-up (mean = 61 months, range 60-96), all individuals were free from episodes of paroxysmal hypothermia independently from previous AED use or other drug therapy.CONCLUSION:
Paroxysmal hypothermia, the core symptom of SS, behaved as a age-dependent feature in our cohort, supporting a good long-term prognosis for SS. A prompt diagnosis of SS is crucial to avoid unnecessary diagnostic investigations.Palavras-chave
Texto completo:
1
Coleções:
01-internacional
Base de dados:
MEDLINE
Assunto principal:
Agenesia do Corpo Caloso
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Hiperidrose
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Hipotermia
Tipo de estudo:
Etiology_studies
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Observational_studies
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Prognostic_studies
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Risk_factors_studies
Limite:
Child
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Female
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Humans
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Male
Idioma:
En
Revista:
Eur J Paediatr Neurol
Ano de publicação:
2018
Tipo de documento:
Article