Letter to the Editor

Complications in Diagnosis of Susceptible Cases of Fragile X Syndrome

Abstract

Complications in Diagnosis of Susceptible Cases of Fragile X Syndrome

Moeschler JB, Shevell M (2014). Comprehensive evaluation of the child with intellectual disability or global developmental delays. Pediatrics,134(3):e903-18.

Soltani S, Khosravi B, Salehiniya H (2015). Prevalence of intellectual disability in Iran: Toward a new conceptual framework in data collection. J Res Med Sci, 20(7):714-5.

Soltani Banavandi MJ, Kahrizi K, Behjati F et al (2012). Investigation of Genetic Causes of Intellectual Disability in Kerman Province, South East of Iran. Iran Red Crescent Med J, 14(2):79-85.

Centers for Disease Control and Prevention (CDC) (2002). Delayed diagnosis of fragile X syndrome--United States, 1990-1999. MMWR Morb Mortal Wkly Rep, 51(33):740-742.

Bailey DB Jr, Raspa M, Bishop E, Holiday D (2009). No change in the age of diagnosis for fragile x syndrome: findings from a national parent survey. Pediatrics, 124(2):527-33.

Hersh JH, Saul RA, Committee on Genetics (2011). Health Supervision for Children With Fragile X Syndrome. Pediatrics, 127(5):994-1006.

Levenson D (2014). Facial analysis technology aids diagnoses of genetic disorders: applications narrow down potential genetic syndromes by matching facial phenotypes to distinct set of possible genetic conditions. Am J Med Genet A, 164A(10):vii-viii.

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How to Cite
1.
JAFARZADEH ESFEHANI R, DASTPAK M, MIRINEZHAD MR, SADR-NABAVI A. Complications in Diagnosis of Susceptible Cases of Fragile X Syndrome. Iran J Public Health. 2018;47(7):1058-1060.