Comportamento angular do andar de crianças com síndrome de Down após intervenção com equoterapia / Angular kinematics of the gait of children with Down's syndrome after intervention with hippotherapy

OBJETIVO: Verificar o efeito de um programa de equoterapia no comportamento angular do tornozelo e joelho de crianças com síndrome de Down (SD). MÉTODO: Fizeram parte do estudo três crianças do sexo masculino com média de idade de 7,3 anos (±2,08). As análises foram realizadas intra-sujeitos, sendo o pós-teste realizado após treze sessões de tratamento. As intervenções com equoterapia tiveram duração de cinqüenta minutos, com intervalos de sete dias. A análise do andar foi realizado pelo Sistema Peak MotusTM. RESULTADOS: Observaram-se alterações significativas para a articulação do tornozelo para todos os sujeitos. Para a articulação do joelho, diferenças foram verificadas em momentos distintos do ciclo, não apresentando uma tendência observável. CONCLUSÃO: A equoterapia promoveu alterações positivas no comportamento angular da articulação do tornozelo, com pouco efeito sobre o joelho.

OBJECTIVE: To investigate the effect of a program of horseback riding therapy on the angular kinematics of the ankle and knee in children with Down's syndrome. METHOD: The study group was composed of three male children with a mean age of 7.3 years (±2.08). The analyses were done individually and the post-test was performed after thirteen treatment sessions. The duration of each horseback riding therapy session was fifty minutes, and the interval between sessions was seven days. The gait analysis was carried out using the Peak MotusTM system. RESULTS: Statistical differences in ankle joint were observed for all subjects. For knee joint, differences were found at different moments of the cycle, without presenting any observable trend. CONCLUSION: Horseback riding therapy produced positive changes in the angular behavior of the ankle and little effect on the knee.

Idiopathic hypertrophic cervical pachymeningitis: a case report with 5 year follow up.

Idiopathic hypertrophic pachymeningitis is an extremely rare entity. It usually affects cranial meninges. The spinal form is further uncommon and presents as a chronic progressive disease. We describe a 42 year old female with isolated idiopathic hypertrophic cervical pachymeningitis who had a relapsing remitting course under observation for five years. Laminectomy and immunosuppressive therapy produced temporary and partial relief. The long term course and relevant literature is reviewed.

Gelastic epilepsy--a case report with SPECT studies.

A 24 years male presented with daily episodes of uncontrollable laughter followed by urinary incontinence since the age of nine years. Some of these attacks progressed to generalized tonic-clonic seizures. General and neurological examination did not reveal any abnormality. Ictal and interictal video EEGs were normal. MRI showed a hypothalamic hamartoma. Interictal SPECT scan showed normal perfusion in the hamartoma. SPECT scan obtained four minutes after beginning of seizure showed that the perfusion increased in right cingulate gyrus but not in the hamartoma, suggesting the involvement of the cingulate gyrus in the seizure origin or pathway.