Common Clinical Characteristics and Rare Medical Problems of Fragile X Syndrome in Thai Patients and Review of the Literature
Autor: | Juthamas Wirojanan, Somchit Jaruratanasirikul, Chariyawan Charalsawadi, Nichara Ruangdaraganon, Pornprot Limprasert, Alan Geater |
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Rok vydání: | 2017 |
Předmět: |
Medulloblastoma
medicine.medical_specialty Pediatrics Article Subject Intelligence quotient Macroorchidism business.industry lcsh:RJ1-570 Cytogenetics lcsh:Pediatrics medicine.disease Fragile X syndrome 03 medical and health sciences 0302 clinical medicine Sample size determination 030225 pediatrics Pediatrics Perinatology and Child Health medicine Attention deficit business 030217 neurology & neurosurgery Research Article Tetralogy of Fallot |
Zdroj: | International Journal of Pediatrics, Vol 2017 (2017) International Journal of Pediatrics |
ISSN: | 1687-9759 1687-9740 |
Popis: | Background. Clinical characteristics of fragile X syndrome (FXS) have been well documented in Caucasians, whereas in Asians they have rarely been described. Those that have been conducted used small cohorts that utilized DNA for diagnosis and larger cohorts that utilized cytogenetics for diagnosis. This study is to describe clinical characteristics of FXS in a large cohort of Thai patients diagnosed by standard molecular methods. Methods. Seventy-seven index cases and 46 affected relatives diagnosed with FXS were recruited into the study. To determine frequencies of common characteristics of FXS in prepubertal boys, we reviewed 56 unrelated cases aged between 18 and 146 months. To list rare medical problems, we reviewed 75 cases aged between 8 months to 71 years old, including 53 index cases and 22 affected relatives. In addition, we selected 16 clinical studies from various ethnicities for comparison with our findings. Results. In prepubertal boys with FXS, attention deficit and/or hyperactivity, prominent ears, macroorchidism, and elongated face were observed in 96%, 80%, 53%, and 48% of patients, respectively, whereas recognizable X-linked inheritance presented in 11% of patients. IQ scores ranged between 30 and 64 (mean ± SD = 43±9, n=25). We observed clinical findings that rarely or have never been reported, for example, medulloblastoma and tetralogy of Fallot. Conclusion. Attention deficit and/or hyperactivity and prominent ear are the most common behavioral and physical features in prepubertal boys with FXS, respectively. There are differences in frequencies of clinical characteristics observed between ethnicities; however, it is difficult to draw a solid conclusion due to different recruitment criteria and sample sizes within each study. |
Databáze: | OpenAIRE |
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