Síndrome de Rett
Palavras-chave:
Síndrome de Rett, autismo, diagnóstico diferencialResumo
A Síndrome de Rett é uma doença degenerativa que acomete meninas, caracterizada por movimentos estereotipados das mãos, padrões respiratórios desordenados e perda das capacidades motora e da linguagem. Os autores descrevem um caso bastante ilustrativo da Síndrome de Rett , detectado em uma criança de três anos. o diagnóstico é essencialmente clínico, tendo sido destacados os critérios de Hagberg e os diagnósticos diferenciados para a Síndrome.
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Referências
HAGBERG, B.,GOUTIERS, F., HANEFELD, F. Rett Syndrome: criteria for inclusion, and exclusion. Brain and Development, Tokyo, v. 1, p. 372-373, 1985.
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HOLM, V.A. Physical crowth and development in patients with Rett Syndrome. American Journal of Medical Genetics, New York, V. 24, p. 119-126, 1986.
MICHAEL, S., ALDRICH, W.D., GAROFALO, E.:, ARBOR, A. Mi epleptiform abnormalities during sleep in Rett Syndrome. Neurology, Cleveland, p. 38, 1988. suppl. 1.
NOMURA, Y., MASSAYA, S. Characteristics of motor disturbances of the Rett Syndrome. Brain and Development, Tokyo, v. 12, p. 27-30, 1990.
PERCY, A., ZOGHBI, H.Y., LEWIS, K.R., JANKOVIK, J. Rett Syndrome: motor and behavioral differentiation from autism. Neurology, Cleveland, v. 37, p. 220, 1987. suppl. 1.
RETT Syndrome diagnostic criteria work group diagnostic criteria for Rett Syndrome (The). Annals of Neurology, Boston, v. 23, p. 425-428. 1988.
ROSEMBERG, S. Clinicai analysis in nine Brasilian cases ofthe Rett Syndrome. Brain and Development, Tokyo, v. 12, p. 44-46, 1990.
ARITA, F.N., CAMPOS, C. A brazilian girl with the Rett Syndrome. Brain and Development, Tokyo, v. 8, p. 552-553, 1986.
