Fragile X syndrome

Emma Hare; Reymundo Lozano; Lindsey Partington; Randi J. Hagerman

doi:10.1007/978-3-319-18096-0_64

Fragile X syndrome

Emma Hare, Reymundo Lozano, Lindsey Partington, Randi J. Hagerman

Pediatrics

Research output: Chapter in Book/Report/Conference proceeding › Chapter

1 Scopus citations

Abstract

Fragile X syndrome and the associated disorders account for a wide range of clinical symptoms that require proper behavioral and pharmacological intervention. Early diagnosis is crucial to maximizing successful interventions and once one child is diagnosed, families should be referred for genetic counseling to establish the possible implications for additional family members and future family planning. This section reviews the phenotypes and neurobiology of the full mutation and premutation as well as possible potential interventions for both sets of patients.

Original language	English (US)
Title of host publication	Health Care for People with Intellectual and Developmental Disabilities Across the Lifespan
Publisher	Springer International Publishing
Pages	751-764
Number of pages	14
ISBN (Electronic)	9783319180960
ISBN (Print)	9783319180953
DOIs	https://doi.org/10.1007/978-3-319-18096-0_64
State	Published - Jan 1 2016

ASJC Scopus subject areas

Medicine(all)
Social Sciences(all)
Psychology(all)

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10.1007/978-3-319-18096-0_64

Cite this

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Fragile X syndrome

Abstract

ASJC Scopus subject areas

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