A clinical series using intensive neurorehabilitation to promote functional motor and cognitive skills in three girls with CASK mutation

Abstract Objectives Children with microcephaly face lifelong psychomotor, cognitive, and communications skills disabilities. Etiology of microcephaly is heterogeneous but presentation often includes seizures, hypotonia, ataxia, stereotypic movements, attention deficits, excitability, cognitive delay...

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Main Authors: Stephanie C. DeLuca, Dory A. Wallace, Mary Rebekah Trucks, Konark Mukherjee
Format: Article
Language:English
Published: BMC 2017-12-01
Series:BMC Research Notes
Subjects:
Online Access:http://link.springer.com/article/10.1186/s13104-017-3065-z
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spelling doaj-7c2ffa38a0af497fa97aaafccae9b0142020-11-25T02:22:58ZengBMCBMC Research Notes1756-05002017-12-011011610.1186/s13104-017-3065-zA clinical series using intensive neurorehabilitation to promote functional motor and cognitive skills in three girls with CASK mutationStephanie C. DeLuca0Dory A. Wallace1Mary Rebekah Trucks2Konark Mukherjee3Virginia Tech Carilion Research InstituteVirginia Tech Carilion Research InstituteVirginia Tech Carilion Research InstituteVirginia Tech Carilion Research InstituteAbstract Objectives Children with microcephaly face lifelong psychomotor, cognitive, and communications skills disabilities. Etiology of microcephaly is heterogeneous but presentation often includes seizures, hypotonia, ataxia, stereotypic movements, attention deficits, excitability, cognitive delays, and poor communication skills. Molecular diagnostics have outpaced available interventions and most children receive generic physical, speech, and occupational therapies with little attention to the efficacy of such treatments. Mutations in the X-linked intellectual disability gene (XLID) CASK is one etiology associated with microcephaly which produces mental retardation and microcephaly with pontine and cerebellar hypoplasia (MICPCH; OMIM# 300749). We pilot-tested an intensive therapy in three girls with heterozygous mutation in the gene CASK and MICPCH. Child A = 54 months; Child B = 89 months; and Child C = 24 months received a targeted treatment to improve gross/fine motor skills, visual-motor coordination, social interaction, and communication. Treatment was 4 h each weekday for 10 treatment days. Operant training promoted/refined goal-directed activities. The Peabody Developmental Motor Scales 2 was administered pre- and post-treatment. Results Child A gained 14 developmental months; Child B gained 20 developmental months; and Child C gained 39 developmental months. This case series suggests that children with MICPCH are responsive to intensive therapy aimed at increasing functional skills/independence. Trial Registration ClinicalTrials.gov Registration Number: NCT03325946; Release Date: October 30, 2017http://link.springer.com/article/10.1186/s13104-017-3065-zMicrocephalyIntellectual disabilityNeurorehabilitationNeuroplasticity
collection DOAJ
language English
format Article
sources DOAJ
author Stephanie C. DeLuca
Dory A. Wallace
Mary Rebekah Trucks
Konark Mukherjee
spellingShingle Stephanie C. DeLuca
Dory A. Wallace
Mary Rebekah Trucks
Konark Mukherjee
A clinical series using intensive neurorehabilitation to promote functional motor and cognitive skills in three girls with CASK mutation
BMC Research Notes
Microcephaly
Intellectual disability
Neurorehabilitation
Neuroplasticity
author_facet Stephanie C. DeLuca
Dory A. Wallace
Mary Rebekah Trucks
Konark Mukherjee
author_sort Stephanie C. DeLuca
title A clinical series using intensive neurorehabilitation to promote functional motor and cognitive skills in three girls with CASK mutation
title_short A clinical series using intensive neurorehabilitation to promote functional motor and cognitive skills in three girls with CASK mutation
title_full A clinical series using intensive neurorehabilitation to promote functional motor and cognitive skills in three girls with CASK mutation
title_fullStr A clinical series using intensive neurorehabilitation to promote functional motor and cognitive skills in three girls with CASK mutation
title_full_unstemmed A clinical series using intensive neurorehabilitation to promote functional motor and cognitive skills in three girls with CASK mutation
title_sort clinical series using intensive neurorehabilitation to promote functional motor and cognitive skills in three girls with cask mutation
publisher BMC
series BMC Research Notes
issn 1756-0500
publishDate 2017-12-01
description Abstract Objectives Children with microcephaly face lifelong psychomotor, cognitive, and communications skills disabilities. Etiology of microcephaly is heterogeneous but presentation often includes seizures, hypotonia, ataxia, stereotypic movements, attention deficits, excitability, cognitive delays, and poor communication skills. Molecular diagnostics have outpaced available interventions and most children receive generic physical, speech, and occupational therapies with little attention to the efficacy of such treatments. Mutations in the X-linked intellectual disability gene (XLID) CASK is one etiology associated with microcephaly which produces mental retardation and microcephaly with pontine and cerebellar hypoplasia (MICPCH; OMIM# 300749). We pilot-tested an intensive therapy in three girls with heterozygous mutation in the gene CASK and MICPCH. Child A = 54 months; Child B = 89 months; and Child C = 24 months received a targeted treatment to improve gross/fine motor skills, visual-motor coordination, social interaction, and communication. Treatment was 4 h each weekday for 10 treatment days. Operant training promoted/refined goal-directed activities. The Peabody Developmental Motor Scales 2 was administered pre- and post-treatment. Results Child A gained 14 developmental months; Child B gained 20 developmental months; and Child C gained 39 developmental months. This case series suggests that children with MICPCH are responsive to intensive therapy aimed at increasing functional skills/independence. Trial Registration ClinicalTrials.gov Registration Number: NCT03325946; Release Date: October 30, 2017
topic Microcephaly
Intellectual disability
Neurorehabilitation
Neuroplasticity
url http://link.springer.com/article/10.1186/s13104-017-3065-z
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