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Growth hormone deficiency and cerebral palsy

Cerebral palsy (CP) is a catastrophic acquired disease, occurring during development of the fetal or infant brain. It mainly affects the motor control centres of the developing brain, but can also affect cognitive functions, and is usually accompanied by a cohort of symptoms including lack of commun...

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Autores principales: Devesa, Jesús, Casteleiro, Nerea, Rodicio, Cristina, López, Natalia, Reimunde, Pedro
Formato: Texto
Lenguaje:English
Publicado: Dove Medical Press 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2940749/
https://www.ncbi.nlm.nih.gov/pubmed/20856687
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author Devesa, Jesús
Casteleiro, Nerea
Rodicio, Cristina
López, Natalia
Reimunde, Pedro
author_facet Devesa, Jesús
Casteleiro, Nerea
Rodicio, Cristina
López, Natalia
Reimunde, Pedro
author_sort Devesa, Jesús
collection PubMed
description Cerebral palsy (CP) is a catastrophic acquired disease, occurring during development of the fetal or infant brain. It mainly affects the motor control centres of the developing brain, but can also affect cognitive functions, and is usually accompanied by a cohort of symptoms including lack of communication, epilepsy, and alterations in behavior. Most children with cerebral palsy exhibit a short stature, progressively declining from birth to puberty. We tested here whether this lack of normal growth might be due to an impaired or deficient growth hormone (GH) secretion. Our study sample comprised 46 CP children, of which 28 were male and 18 were female, aged between 3 and 11 years. Data obtained show that 70% of these children lack normal GH secretion. We conclude that GH replacement therapy should be implemented early for CP children, not only to allow them to achieve a normal height, but also because of the known neurotrophic effects of the hormone, perhaps allowing for the correction of some of the common disabilities experienced by CP children.
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spelling pubmed-29407492010-09-20 Growth hormone deficiency and cerebral palsy Devesa, Jesús Casteleiro, Nerea Rodicio, Cristina López, Natalia Reimunde, Pedro Ther Clin Risk Manag Original Research Cerebral palsy (CP) is a catastrophic acquired disease, occurring during development of the fetal or infant brain. It mainly affects the motor control centres of the developing brain, but can also affect cognitive functions, and is usually accompanied by a cohort of symptoms including lack of communication, epilepsy, and alterations in behavior. Most children with cerebral palsy exhibit a short stature, progressively declining from birth to puberty. We tested here whether this lack of normal growth might be due to an impaired or deficient growth hormone (GH) secretion. Our study sample comprised 46 CP children, of which 28 were male and 18 were female, aged between 3 and 11 years. Data obtained show that 70% of these children lack normal GH secretion. We conclude that GH replacement therapy should be implemented early for CP children, not only to allow them to achieve a normal height, but also because of the known neurotrophic effects of the hormone, perhaps allowing for the correction of some of the common disabilities experienced by CP children. Dove Medical Press 2010 2010-09-07 /pmc/articles/PMC2940749/ /pubmed/20856687 Text en © 2010 Devesa et al, publisher and licensee Dove Medical Press Ltd. This is an Open Access article which permits unrestricted noncommercial use, provided the original work is properly cited.
spellingShingle Original Research
Devesa, Jesús
Casteleiro, Nerea
Rodicio, Cristina
López, Natalia
Reimunde, Pedro
Growth hormone deficiency and cerebral palsy
title Growth hormone deficiency and cerebral palsy
title_full Growth hormone deficiency and cerebral palsy
title_fullStr Growth hormone deficiency and cerebral palsy
title_full_unstemmed Growth hormone deficiency and cerebral palsy
title_short Growth hormone deficiency and cerebral palsy
title_sort growth hormone deficiency and cerebral palsy
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2940749/
https://www.ncbi.nlm.nih.gov/pubmed/20856687
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