Neuropsychological findings in Hamamy syndrome: A clinical case report

dc.contributor.authorRoukoz, Cynthia
dc.contributor.authorKanj, Rama Rand
dc.contributor.authorMaalouf, Fadi T.
dc.contributor.authorZeinoun, Pia
dc.contributor.departmentPsychiatry
dc.contributor.departmentDepartment of Education
dc.contributor.departmentDepartment of Psychology
dc.contributor.facultyFaculty of Medicine (FM)
dc.contributor.facultyFaculty of Arts and Sciences (FAS)
dc.contributor.institutionAmerican University of Beirut
dc.date.accessioned2025-01-24T12:11:55Z
dc.date.available2025-01-24T12:11:55Z
dc.date.issued2019
dc.description.abstractThis study, reports for the first time, the neuropsychological profile of a child with Hamamy syndrome- A rare genetic disorder with only five published cases (Buget, Canbolat, Akgul, & Kucukay, 2015). The patient was seen for a neuropsychological evaluation at ages 6 and 7, at the American University of Beirut Medical Center. Procedures included an extended clinical interview with the parent, behavioral observations, formal tests, and a series of parental rating scales. Patient was found to have relatively spared nonverbal intelligence, borderline-impaired language, and clinically impaired verbal reasoning, attention, and motor coordination. Additionally, he showed clinically significant concerns with behavioral regulation, metacognition, attention-deficit, and hyperactivity/impulsivity. The patient was diagnosed with a DSM-V Language Disorder, Speech Sound Disorder, and Attention Deficit/Hyperactivity Disorder, combined presentation, in the context of low-average intelligence. At follow-up, the neuropsychological profile was consistent, albeit improvement was noted following pharmacotherapy. This is the first published report that describes the neuropsychological functions of Hamamy syndrome. We make recommendations for early identification of cognitive strengths and weaknesses, and interventions to address them. Future research should evaluate additional functions such as memory and social/emotional development. © 2019 The International Neuropsychological Society.
dc.identifier.doihttps://doi.org/10.1017/S1355617718001133
dc.identifier.eid2-s2.0-85061274910
dc.identifier.pmid30729910
dc.identifier.urihttp://hdl.handle.net/10938/32618
dc.language.isoen
dc.publisherCambridge University Press
dc.relation.ispartofJournal of the International Neuropsychological Society
dc.sourceScopus
dc.subjectHamamy syndrome
dc.subjectNeuropsychological profile
dc.subjectRare genetic disorder
dc.subjectAttention deficit disorder with hyperactivity
dc.subjectBone diseases
dc.subjectChild
dc.subjectHumans
dc.subjectHypertelorism
dc.subjectIntellectual disability
dc.subjectIntelligence
dc.subjectLanguage disorders
dc.subjectMale
dc.subjectMyopia
dc.subjectSpeech disorders
dc.subjectAttention deficit disorder
dc.subjectBone disease
dc.subjectCase report
dc.subjectComplication
dc.subjectHuman
dc.subjectIntellectual impairment
dc.subjectLanguage disability
dc.subjectPathophysiology
dc.subjectPhysiology
dc.subjectSpeech disorder
dc.titleNeuropsychological findings in Hamamy syndrome: A clinical case report
dc.typeArticle

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