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1.
Cephalalgia ; 37(12): 1202-1206, 2017 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-27651281

RESUMO

Introduction Variants in the CACNA1A gene on chromosome 19p13 result in a spectrum of neurological phenotypes ranging from familial or sporadic hemiplegic migraine to congenital or progressive encephalopathies. Patients with CACNA1A variants often show acute attacks with ataxia or hemiplegia till coma, sometimes related to unilateral brain oedema. No guidelines for the medical management of these attacks are available since treatment is empiric, and many cases do not respond to common antimigraine drugs. Case description We report on the emergency personalized treatment protocol used in an 11 year-old girl with CACNA1A-related encephalopathy for the management of acute attacks of headache, hemiconvulsions and hemiplegia with coma. Discussion Combined corticosteroid pulses and hypertonic solution led to a reduction in severity and duration of acute attacks when administered in the early stages, characterized by migraine, seizure, fever, vomiting and impairment of consciousness associated to hemispheric slowing on the EEG.


Assuntos
Anticonvulsivantes/uso terapêutico , Edema Encefálico/tratamento farmacológico , Glucocorticoides/uso terapêutico , Enxaqueca com Aura/tratamento farmacológico , Edema Encefálico/genética , Canais de Cálcio/genética , Criança , Dexametasona/uso terapêutico , Toxidermias/etiologia , Feminino , Frutose/análogos & derivados , Frutose/uso terapêutico , Humanos , Lamotrigina , Enxaqueca com Aura/genética , Mutação de Sentido Incorreto , Topiramato , Triazinas/efeitos adversos
2.
Metab Brain Dis ; 30(3): 681-6, 2015 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-25156245

RESUMO

Mucolipidosis type IV (MLIV) is a very rare disorder of late endosome/lysosome transport, characterized by neurodevelopmental abnormalities and progressive visual impairment owing to corneal clouding and retinal dystrophy. Greater than 70 % of MLIV patients are of Ashkenazi Jewish ancestry. Here we report a novel MCOLN1double mutant allele [c.395_397delCTG;c.468_474dupTTGGACC] which introduces a premature stop codon [p.Ala132del; p.Asn159LeufsX27] leading to almost complete abrogation of the region coding mucolipin-1, a member of the transient receptor potential (TRP) cation channel family. The genomic lesion was identified in homozygous state, in a non-Jewish Italian MLIV patient, who also presented abnormal serum gastrin levels. Conventional and advanced MRI sequences, including diffusion tensor imaging and tractography, were used for the assessment of white matter involvement in the patient.


Assuntos
Alelos , Mucolipidoses/genética , Mutação/genética , Canais de Potencial de Receptor Transitório/genética , População Branca/genética , Pré-Escolar , Homozigoto , Humanos , Itália , Masculino , Mucolipidoses/diagnóstico , Canais de Potencial de Receptor Transitório/deficiência
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