Secondary medical diagnosis in fragile X syndrome with and without autism spectrum disorder

C García‐Nonell, ER Ratera, S Harris… - American Journal of …, 2008 - Wiley Online Library
C García‐Nonell, ER Ratera, S Harris, D Hessl, MY Ono, N Tartaglia, E Marvin, F Tassone
American Journal of Medical Genetics Part A, 2008Wiley Online Library
This study examined whether secondary medical diagnoses that affect CNS function (ie,
seizures, malformations, or genetic disorders), are more likely to occur in individuals with
fragile X syndrome (FXS) and autism spectrum disorder (FXS+ ASD) or FXS alone. Ninety
males (3–25 years) with FXS or FXS+ ASD were evaluated for secondary medical
diagnoses by medical history and examination. A significant difference in the incidence of
medical problems was found between patients with FXS+ ASD (38.6%) and FXS alone …
Abstract
This study examined whether secondary medical diagnoses that affect CNS function (i.e., seizures, malformations, or genetic disorders), are more likely to occur in individuals with fragile X syndrome (FXS) and autism spectrum disorder (FXS + ASD) or FXS alone. Ninety males (3–25 years) with FXS or FXS + ASD were evaluated for secondary medical diagnoses by medical history and examination. A significant difference in the incidence of medical problems was found between patients with FXS + ASD (38.6%) and FXS alone (18.2%, P < 0.05). Medical problems that affect the CNS are more likely to occur in those with FXS + ASD and it is probable that additional brain dysfunction associated with these medical problems enhance the risk of autism in those with FXS. © 2008 Wiley‐Liss, Inc.
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