Your browser doesn't support javascript.
loading
Síndrome de X frágil: análisis clínico en 300 pacientes con retardo mental inespecífico en la población chilena / Fragile X syndrome: clinical analysis of 300 Chilean patients with unspecific mental retardation
Rev. méd. Chile ; 126(12): 1447-54, dic. 1998. ilus
Article em Es | LILACS | ID: lil-243741
Biblioteca responsável: CL1.1
ABSTRACT

Background:

Fragile X syndrome is the most important cause of sex linked mental retardation and the second of chromosomal origin, after Down syndrome.

Aim:

To apply the modified Hagerman score to patients with mental retardation and to relate clinical findings with cytogenetic and molecular diagnosis. Patients and

methods:

The modified Hagerman score was applied to 214 male and 86 female patients with mental retardation. The clinical variables in non fragile X and fragile X cases, determined by molecular and cytogenetic methods, were compared.

Results:

The score in 210 non fragile X males was 10.5 + 3.7 (range 3 23), compared to 21.4 + 2.1 (range 19 to 23) in the four fragile X patients. All fragile X patients had mental retardation, attention deficits, hyperactivity disorders, hand biting and poor visual contact. Hand biting, flapping and persevering speech were observed in a significantly higher number of fragile X males. Only one of 86 females had fragile X syndrome. Her most relevant findings were a long face and high forehead, an attention deficit, hyperactivity and poor visual contact. No clinical differences with other mentally retarded females were found. Condusions Approximately 5 percent of institutionalized males with mental retardation have a fragile X syndrome
Assuntos
Buscar no Google
Índice: LILACS Assunto principal: Síndrome do Cromossomo X Frágil / Deficiência Intelectual Tipo de estudo: Etiology_studies Limite: Adolescent / Adult / Female / Humans / Male País/Região como assunto: America do sul / Chile Idioma: Es Revista: Rev. méd. Chile Assunto da revista: MEDICINA Ano de publicação: 1998 Tipo de documento: Article / Project document
Buscar no Google
Índice: LILACS Assunto principal: Síndrome do Cromossomo X Frágil / Deficiência Intelectual Tipo de estudo: Etiology_studies Limite: Adolescent / Adult / Female / Humans / Male País/Região como assunto: America do sul / Chile Idioma: Es Revista: Rev. méd. Chile Assunto da revista: MEDICINA Ano de publicação: 1998 Tipo de documento: Article / Project document