Complications in Diagnosis of Susceptible Cases of Fragile X Syndrome

  • Reza JAFARZADEH ESFEHANI Dept. of Medical Genetics, School of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran Medical Genetic Research Center, School of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran
  • Mahtab DASTPAK Dept. of Genetic, Academic Center for Education, Culture, and Research (ACECR), Mashhad, Iran Stem Cell and Regenerative Medicine Research Group, Academic Center for Education, Culture and Research (ACECR), Khorasan Razavi Branch, Mashhad, Iran
  • Mohammad Reza MIRINEZHAD Dept. of Medical Genetics, School of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran Medical Genetic Research Center, School of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran
  • Ariane SADR-NABAVI Dept. of Medical Genetics, School of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran Medical Genetic Research Center, School of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran Dept. of Genetic, Academic Center for Education, Culture, and Research (ACECR), Mashhad, Iran
Keywords: No keywords##

Abstract

Complications in Diagnosis of Susceptible Cases of Fragile X Syndrome

References

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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.

Published
2018-07-16
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. 47(7):1058-1060.
Section
Letter to the Editor