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Neuropsychological, psychiatric, and physical manifestations in 149 members from 18 fragile X families.
Cianchetti, C; Sannio-Fancello, G; Fratta, A L; Manconi, F; Orano, A; Pischedda, M P; Pruna, D; Spinicci, G; Archidiacono, N; Filippi, G.
Afiliação
  • Cianchetti C; Istituto di Neuropsichiatria Infantile, Università di Cagliari, Italy.
Am J Med Genet ; 40(2): 234-43, 1991 Aug 01.
Article em En | MEDLINE | ID: mdl-1897579
ABSTRACT
One hundred forty-nine subjects from 18 families with fragile X [fra(X)] syndrome were evaluated for their neuropsychological, psychiatric, and physical characteristics. The 36 fra(X) males had intelligence quotients ranging from less than 20 to 61, which prevented the delineation of a reliable neuropsychological profile. Behaviour fitted DSM-III-R and ADI diagnostic criteria of autism in only 2 subjects, both with very low intelligence level (IQ less than 20). Of 36 heterozygotes (HZ), 22 had an IQ between 20 and 80 and 14 between 81 and 99. The neuropsychological profile of the latter was compared with IQ-age-environment-matched 14 normal females and 14 normal males. Significantly poorer results in HZ were found on immediate digit memory and on Raven's progressive matrices (a visuo-spatial test of logical capabilities). The latter result, in conjunction with those results on the Bender visual-motor gestalt test and on some WAIS subtests, suggests a frequent deficit in spatial capabilities in such subjects. Such results tended to be confirmed by the profiles of the 22 HZ with IQ 20-80. No psychiatric abnormalities were found in HZ, except in one subject with IQ less than 20 which fitted DSM-III-R and ADI criteria for autism. Typical physical manifestations, especially cranio-facial, were more frequently present in the HZ group with lower IQ. Subnormal IQ was probably the most reliable abnormality for the detection of HZ in 49 females at 50% and 25% risk of heterozygosity.
Assuntos
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Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndrome do Cromossomo X Frágil / Heterozigoto / Inteligência Limite: Adolescent / Adult / Aged / Child / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 1991 Tipo de documento: Article
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Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndrome do Cromossomo X Frágil / Heterozigoto / Inteligência Limite: Adolescent / Adult / Aged / Child / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 1991 Tipo de documento: Article