dc.creatorAspillaga, Manuel H.
dc.creatorJara, Lilian S.
dc.creatorAvendaño, Isabel B.
dc.creatorLópez, Maribel S.
dc.date.accessioned2019-01-29T17:16:05Z
dc.date.available2019-01-29T17:16:05Z
dc.date.created2019-01-29T17:16:05Z
dc.date.issued1998
dc.identifierRevista Medica de Chile, Volumen 126, Issue 12, 2018, Pages 1447-1454
dc.identifier00349887
dc.identifierhttp://repositorio.uchile.cl/handle/2250/163400
dc.description.abstractBackground: 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 perserering speech were observed in a significantly higher number of fragile X males. Only one of 86 females had fragile X syndrome. Her most releva
dc.languageen
dc.rightshttp://creativecommons.org/licenses/by-nc-nd/3.0/cl/
dc.rightsAttribution-NonCommercial-NoDerivs 3.0 Chile
dc.sourceRevista Medica de Chile
dc.subjectChromosome abnormalities
dc.subjectCytogenetics
dc.subjectFragile X syndrome
dc.subjectMental retardation
dc.titleFragile X syndrome. Clinical analysis of 300 Chilean patients with unspecific mental retardation Síndrome de X frágil. Análisis clínico en 300 pacientes con retardo mental inespecífico en la población chilena
dc.typeArtículos de revistas


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