RESUMO
Paroxysmal kinesigenic dyskinesia (PKD) is a rare disorder characterised by brief and frequent attacks of abnormal involuntary movements induced by sudden movement. This disorder has not been reported previously in Sri Lanka. We studied six patients with respect to clinical presentation, aetiology, family history and response to treatment, and describe the Sri Lankan patterns of this illness. All the patients were males and the age at onset was from 11 to 22 years. The involuntary movements in all were dystonic and affected one or both sides, involving the face in the majority. All had difficulty in speaking during the attacks. One patient had an occasional attack during exercise. In all, the illness was sporadic, none had a family history of a similar illness and in none was it due to a secondary cause. The attacks usually lasted 10-60 seconds, and occurred up to 20 times a day. All patients responded well to anticonvulsants. PKD in Sri Lanka has a pattern similar to that described worldwide.
Assuntos
Distonia/diagnóstico , Adolescente , Adulto , Fatores Etários , Anticonvulsivantes/uso terapêutico , Tronco Encefálico , Criança , Distonia/tratamento farmacológico , Epilepsia/fisiopatologia , Humanos , Masculino , Córtex Motor , Sri LankaAssuntos
Infarto Cerebral/etiologia , Hemianopsia/etiologia , Hemoglobinúria Paroxística/complicações , Hiper-Homocisteinemia/complicações , Paresia/etiologia , Deficiência de Proteína C/complicações , Acidente Vascular Cerebral/etiologia , Adulto , Fatores Etários , Causalidade , Infarto Cerebral/diagnóstico , Ecocardiografia , Hemianopsia/diagnóstico , Hemoglobinúria Paroxística/diagnóstico , Hemoglobinúria Paroxística/genética , Humanos , Hiper-Homocisteinemia/diagnóstico , Hiper-Homocisteinemia/genética , Masculino , Paresia/diagnóstico , Deficiência de Proteína C/diagnóstico , Deficiência de Proteína C/genética , Acidente Vascular Cerebral/diagnóstico , Tomografia Computadorizada por Raios XRESUMO
We describe a case of hereditary sensory and autonomic neuropathy (HSAN) type II in a child with a penetrating foot ulcer, acral sensory impairment, and anhidrosis. This is the first documentation of HSAN in Sri Lanka.
Assuntos
Úlcera do Pé/etiologia , Neuropatias Hereditárias Sensoriais e Autônomas/diagnóstico , Neurônios Aferentes/patologia , Potenciais de Ação , Criança , Diagnóstico Diferencial , Neuropatias Hereditárias Sensoriais e Autônomas/complicações , Neuropatias Hereditárias Sensoriais e Autônomas/patologia , Neuropatias Hereditárias Sensoriais e Autônomas/fisiopatologia , Humanos , Hipo-Hidrose/etiologia , Masculino , Fibras Nervosas Mielinizadas/patologia , Nervo Sural/fisiopatologia , Nervo Ulnar/fisiopatologiaAssuntos
Síndrome de Guillain-Barré/diagnóstico , Nervo Sural/patologia , Doença Aguda , Idoso , Axônios/patologia , Biópsia , Diagnóstico Diferencial , Evolução Fatal , Síndrome de Guillain-Barré/complicações , Síndrome de Guillain-Barré/patologia , Síndrome de Guillain-Barré/fisiopatologia , Humanos , Síndrome de Secreção Inadequada de HAD/etiologia , Masculino , Pessoa de Meia-Idade , Paralisia/etiologiaRESUMO
A case of eosinophilic meningitis is reported, a condition not previously reported from Sri Lanka. We propose Angiostrongylus cantonesis to be the most likely causative agent in this patient.