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1.
Am J Med Genet A ; 182(8): 1881-1889, 2020 08.
Artículo en Inglés | MEDLINE | ID: mdl-32220052

RESUMEN

This cross-sectional study examined the neurodevelopment of a large, prenatally diagnosed population of boys with 47,XXY; investigated the potentially positive effects of early hormonal therapy (EHT) on language, cognition, and motor in this population; and identified novel at risk biomarkers associated with 47,XXY. Two-hundred and seventy two evaluations were collected from 148 prenatally diagnosed boys with 47,XXY between 0 and 36 months and separated into one of three groups, depending on visit age: Y1 (0-12 months; n = 100), Y2 (13-24 months; n = 90), and Y3 (25-36 months; n = 82). Those who received EHT (administered by 12 months) were further separated (Y1, n = 37; Y2, n = 34; Y3, n = 30). Neurodevelopmental evaluations consisted of Preschool Language Scales, Early Language Milestone Scale, and Bayley Scales of Infant and Toddler Development and evaluated the effect of EHT on auditory comprehension, expressive communication, receptive language, cognition, and motor. EHT was found to be associated with a positive effect within the first year of life in these domains, as well as in the second and third year of life. Additionally, three novel at-risk biomarkers were identified in this cohort: feeding difficulties in infancy, positional torticollis, and the need for orthotics. The positive effects of EHT observed in language, cognition, and motor at variable stages within the first 3 years of life provide additional evidence into the possible efficacy of early biological treatment for boys with 47,XXY to address the neurodevelopmental dysfunction.


Asunto(s)
Hormonas/administración & dosificación , Síndrome de Klinefelter/tratamiento farmacológico , Diagnóstico Prenatal , Trastornos de los Cromosomas Sexuales/tratamiento farmacológico , Cariotipo XYY/tratamiento farmacológico , Biomarcadores/sangre , Preescolar , Cognición/efectos de los fármacos , Cognición/fisiología , Femenino , Hormonas/efectos adversos , Humanos , Lactante , Síndrome de Klinefelter/diagnóstico , Síndrome de Klinefelter/genética , Síndrome de Klinefelter/fisiopatología , Masculino , Trastornos del Neurodesarrollo/diagnóstico , Trastornos del Neurodesarrollo/epidemiología , Trastornos del Neurodesarrollo/genética , Trastornos del Neurodesarrollo/fisiopatología , Embarazo , Factores de Riesgo , Trastornos de los Cromosomas Sexuales/diagnóstico , Trastornos de los Cromosomas Sexuales/genética , Trastornos de los Cromosomas Sexuales/fisiopatología , Cariotipo XYY/diagnóstico , Cariotipo XYY/genética , Cariotipo XYY/fisiopatología
3.
Am J Med Genet C Semin Med Genet ; 169(2): 150-7, 2015 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-25939399

RESUMEN

47, XXY occurs in up to 1 in 650 male births and is associated with androgen deficiency, neurodevelopmental delays, and atypical social-behaviors. Previously, we showed that young boys with 47, XXY who received early hormonal therapy (EHT) had significantly improved neurodevelopment. The objective of this follow-up study was to examine the effects of EHT on social behavior in boys with 47, XXY. The study consisted of boys prenatally diagnosed with 47, XXY who were referred for evaluations. Twenty-nine boys received three injections of 25 mg testosterone enanthate and 57 controls did not receive EHT. Behavioral functioning was assessed using the Behavior Rating Inventory of Executive Function, Social Responsiveness Scale, 2nd Ed., and the Child Behavior Checklist for Ages 6-18. The hypothesis that EHT may affect behavior was formulated prior to data collection. Questionnaire data was prospectively obtained and analyzed to test for significance between two groups. Significant differences were identified between group's scores over time in Social Communication (P=0.007), Social Cognition (P=0.006), and Total T-score (P=0.001) on the SRS-2; Initiation (P=0.05) on the BRIEF; and Externalizing Problems (P=0.024), Affective Problems (P=0.05), and Aggressive Behaviors (P=0.031) on the CBCL. This is the third study revealing positive effects of EHT on boys with XXY. There was a significant improvements associated with the 47, XXY genotype in boys who received EHT. Research is underway on the neurobiological mechanisms, and later developmental effects of EHT.


Asunto(s)
Andrógenos/uso terapéutico , Discapacidades del Desarrollo/tratamiento farmacológico , Terapia de Reemplazo de Hormonas/métodos , Trastornos de los Cromosomas Sexuales/tratamiento farmacológico , Conducta Social , Testosterona/análogos & derivados , Cariotipo XYY/tratamiento farmacológico , Escala de Evaluación de la Conducta , Estudios de Casos y Controles , Niño , Preescolar , Comunicación , Discapacidades del Desarrollo/diagnóstico , Discapacidades del Desarrollo/fisiopatología , Discapacidades del Desarrollo/psicología , Estudios de Seguimiento , Humanos , Cariotipificación , Masculino , Fenotipo , Diagnóstico Prenatal , Trastornos de los Cromosomas Sexuales/diagnóstico , Trastornos de los Cromosomas Sexuales/fisiopatología , Trastornos de los Cromosomas Sexuales/psicología , Testosterona/uso terapéutico , Resultado del Tratamiento , Cariotipo XYY/diagnóstico , Cariotipo XYY/fisiopatología , Cariotipo XYY/psicología
4.
J Pediatr Hematol Oncol ; 27(12): 688-91, 2005 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-16344680

RESUMEN

Thrombolytic therapy is a well-defined treatment option for arterial and venous thrombosis in adults. In contrast, uniform recommendations regarding the indication, route of administration, and dosing of thrombolytic therapy in children are not available. The authors report the successful resolution of bilateral pulmonary embolism and popliteal artery thrombosis in an 11-year-old girl and 13-year-old girl, respectively, by catheter-directed thrombolysis with low-dose recombinant tissue plasminogen activator. Catheter-directed low-dose thrombolysis is an efficient treatment option for severe venous and arterial thrombosis in children.


Asunto(s)
Fibrinolíticos/uso terapéutico , Arteria Poplítea , Embolia Pulmonar/tratamiento farmacológico , Proteínas Recombinantes/uso terapéutico , Terapia Trombolítica/métodos , Trombosis/tratamiento farmacológico , Activador de Tejido Plasminógeno/uso terapéutico , Adolescente , Factores de Edad , Anticoagulantes/administración & dosificación , Anticoagulantes/uso terapéutico , Artroscopía , Niño , Relación Dosis-Respuesta a Droga , Quimioterapia Combinada , Estrógenos/efectos adversos , Estrógenos/uso terapéutico , Femenino , Fibrinolíticos/administración & dosificación , Hematoma/inducido químicamente , Heparina/administración & dosificación , Heparina/uso terapéutico , Humanos , Inyecciones Intraarteriales , Traumatismos de la Rodilla/cirugía , Lupus Eritematoso Sistémico/sangre , Lupus Eritematoso Sistémico/complicaciones , Fenprocumón/administración & dosificación , Fenprocumón/uso terapéutico , Complicaciones Posoperatorias/tratamiento farmacológico , Complicaciones Posoperatorias/etiología , Progesterona/uso terapéutico , Arteria Pulmonar , Embolia Pulmonar/etiología , Proteínas Recombinantes/administración & dosificación , Proteínas Recombinantes/efectos adversos , Trastornos de los Cromosomas Sexuales/complicaciones , Trastornos de los Cromosomas Sexuales/tratamiento farmacológico , Terapia Trombolítica/instrumentación , Trombofilia/tratamiento farmacológico , Trombofilia/etiología , Trombosis/etiología , Activador de Tejido Plasminógeno/administración & dosificación , Activador de Tejido Plasminógeno/efectos adversos , Trisomía
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