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1.
Einstein (Säo Paulo) ; 16(2): eRC3961, 2018. graf
Article in English | LILACS | ID: biblio-891468

ABSTRACT

ABSTRACT The height response to the use of growth hormone in short height cases has already been confirmed in the literature. The influence of the insulin-like growth factor 1 (GH-IGF1) axis components on development, function, regeneration, neuroprotection, cognition, and motor functions has been evaluated in experimental studies and in adults with central nervous system lesions. However, there is still little research on the clinical impact of hormone replacement on neurological and psychomotor development. This report presents the case of a patient with excellent weight-height recovery and, even more surprisingly, neurological and psychomotor development in response to use of growth hormone. The result strengthens the correlation between experimental and clinical findings related to cerebral plasticity response to growth hormone in children. A preterm male patient with multiple health problems during the neonatal and young infancy period, who for six years presented with a relevant deficit in growth, bone maturation, and neurological and psychomotor development. At six years of age, he had low stature (z-score −6.89), low growth rate, and low weight (z-score −7.91). He was incapable of sustaining his axial weight, had not developed fine motor skills or sphincter control, and presented with dysfunctional swallowing and language. Supplementary tests showed low IGF-11 levels, with no changes on the image of the hypothalamus-pituitary region, and bone age consistent with three-year-old children — for a chronological age of six years and one month. Growth hormone replacement therapy had a strong impact on the weight-height recovery as well as on the neurological and psychomotor development of this child.


RESUMO A resposta estatural ao uso de hormônio do crescimento na baixa estatura já está comprovada na literatura. A influência dos componentes do eixo fator de crescimento semelhante à insulina tipo 1 (GH-IGF1) sobre desenvolvimento, função, regeneração, neuroproteção, cognição e funções motoras tem sido avaliada em estudos experimentais e em adultos com lesão de sistema nervoso central. No entanto, ainda são poucas as pesquisas sobre o impacto clínico da reposição hormonal no desenvolvimento neuropsicomotor. Este relato apresenta o caso de um paciente com excelente recuperação pôndero-estatural e, de forma ainda mais surpreendente, de desenvolvimento neuropsicomotor, em resposta ao uso de hormônio do crescimento. O resultado observado fortalece a correlação entre achados experimentais e clínicos, no que diz respeito à resposta da plasticidade cerebral ao hormônio do crescimento em crianças. Paciente do sexo masculino nasceu pré-termo com múltiplos agravos no período neonatal e de lactente jovem, e que, por 6 anos, apresentou deficit relevante do crescimento, na maturação óssea e do desenvolvimento neuropsicomotor. Aos 6 anos de idade, apresentava baixa estatura (escore Z de −6,89), baixa velocidade de crescimento e baixo peso (escore Z de −7,91). Era incapaz de sustentar o peso axial, não tinha desenvolvido habilidade motora fina e nem controle esfincteriano, e apresentava também disfunção na deglutição e na linguagem. Exames complementares mostraram IGF1 baixo, sem alterações na imagem da região hipotálamo-hipofisária e idade óssea compatível com 3 anos — para a idade cronológica de 6 anos e 1 mês. A terapia de reposição com hormônio do crescimento promoveu forte impacto na recuperação pôndero-estatural e também do desenvolvimento neuropsicomotor desta criança.


Subject(s)
Humans , Male , Child , Child Development/drug effects , Child Development/physiology , Human Growth Hormone/deficiency , Human Growth Hormone/therapeutic use , Hormone Replacement Therapy/methods , Psychomotor Disorders/drug therapy , Time Factors , Body Height/drug effects , Body Height/physiology , Body Weight/drug effects , Body Weight/physiology , Treatment Outcome , Nervous System Diseases/drug therapy
2.
Cir. & cir ; 77(1): 9-12, ene.-feb. 2009. tab
Article in Spanish | LILACS | ID: lil-566696

ABSTRACT

Objetivo: Evaluar los resultados del tratamiento con toxina botulínica en pacientes con endotropía y retraso psicomotor. Material y métodos: Se incluyeron pacientes con endotropía y retraso del desarrollo psicomotor menores de siete años, en tratamiento de rehabilitación y sin cirugía previa. Se les realizó exploración oftalmológica y estrabológica completa incluyendo cicloplejía con atropina a 1 %. Se aplicó toxina botulínica en ambos rectos internos bajo sedación y se evaluaron los resultados a la semana, al mes, a los tres y seis meses y al año. Se decidió reinyección si se obtuvo endotropía residual mayor de 25 dioptrías (dp) antes de los tres meses de la primera aplicación. Se consideró un buen resultado cuando hubo desviación dentro de las 10 dp y variabilidad menor o igual a 10 dp. Resultados: Se incluyeron 32 pacientes, 14 mujeres y 18 hombres. El rango de edad era de cinco meses a cinco años, con un promedio de 16.8 meses. Se encontraron 18 pacientes con variabilidad en el ángulo de desviación de 20 a 45 dp de endotropía y 14 sin variabilidad, con un promedio de 39.12 dp. Se reinyectaron 13 pacientes. En 10 pacientes hubo buen resultado, en 17 regular y en cinco malo. Los malos resultados fueron por persistencia de variabilidad importante en cuatro pacientes y en uno hipertropía mayor de 15 dp.Conclusiones: La aplicación de toxina botulínica es una alternativa terapéutica en pacientes con endotropía y retraso psicomotor.


OBJECTIVE: We undertook this study to evaluate the results of the treatment with botulinum toxin in patients with esotropia and psychomotor delay. METHODS: Patients with esotropia and delayed psychomotor development, in rehabilitation therapy and without previous surgery were included. A complete ophthalmological and strabismological exploration was performed including cycloplegic refraction with atropine 1%. Botulinum toxin was applied under sedation in both internal recti. Results were evaluated 1 week, 1 month, 3 and 6 months and after 1 year of application. The reinjection was decided if a 25 DP esotropia or greater was obtained before 3 months of the first application. A good result was considered in patients who had 10 DP of deviation and variability <10 DP. RESULTS: Thirty two patients were included. There were 14 were women and 18 men with an age range from 5 months to 5 years (average 16.8 months). Eighteen patients had variability in the angle of deviation from 20 to 45 DP of esotropia and 14 without variability with an average of 39.12 DP. Thirteen patients were reinjected. A good result was obtained in 10 patients, fair in 17 patients and poor in 5 patients due to persistence of variability in four cases and 15 DP hypertropia in one. CONCLUSIONS: Application of botulinum toxin is a therapeutic alternative in patients with esotropia and psychomotor delay.


Subject(s)
Humans , Male , Female , Child, Preschool , Infant , Esotropia/drug therapy , Botulinum Toxins/therapeutic use , Psychomotor Disorders/drug therapy , Prospective Studies
3.
Bol. Hosp. San Juan de Dios ; 41(4): 228-37, jul.-ago. 1994. tab, ilus
Article in Spanish | LILACS | ID: lil-140420

ABSTRACT

El síndrome a largo plazo por levodopa (L-Dopa) corresponde a las manifestaciones adversas provocadas por el fármaco, que aparecen generalmente después de un año o más de su empleo y que afectan aproximadamente al 50 por ciento de los casos. Los síntomas son muy variados y polimorfos, los más habituales son de tipo motor (diskinesias, distonías posturales y disminución de la respuesta motora), se agregan otros, como trastornos mentales, neurovegetativos y sensitivos. Para la profilaxis de este síndrome debe considerarse el retraso en la iniciación de la terapia, usándose como alternativa: selegilina, bromocriptina, anticolinérgicos (thihexifenidilo) o antidepresivos. En casos severos de enfermedad de Prkinson y que no pueda obviarse el uso de L-Dopa, ésta debe emplearse inicialmente en la dosis mínima efectiva, la que se aumenta en forma lenta y progresiva en varias semanas. Otra variables es el uso de formulaciones de liberación controlada (Prolopa HBS o Sinemet CR). También es recomendable la asociación de agonistas dopaminérgicos que tendrían un efecto protector en el síndrome a largo plazo de L-Dopa


Subject(s)
Levodopa/adverse effects , Parkinson Disease/drug therapy , Dopamine Agents/administration & dosage , Drug Administration Schedule , Dyskinesia, Drug-Induced/drug therapy , Neurologic Manifestations , Psychomotor Disorders/drug therapy
6.
Rev. serv. sanid. fuerzas polic ; 46(2): 138-41, jul.-dic. 1985.
Article in Spanish | LILACS, LIPECS | ID: lil-27502

ABSTRACT

En el presente artículo se presenta una breve revisión de las indicaciones y de las dosis de los psicofármacos utilizados en los niños. Las indicaciones de los psicofármacos se analizan en función de síndromes infantiles diversos. Las dosis que se incluyen son aquellas recomendadas por diversos autores y especialistas


Subject(s)
Child, Preschool , Child , Adolescent , Humans , Psychomotor Disorders/drug therapy , Psychopharmacology , Child Psychiatry , Depression/drug therapy , Psychotropic Drugs/therapeutic use
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