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1.
Orphanet J Rare Dis ; 14(1): 198, 2019 08 14.
Artículo en Inglés | MEDLINE | ID: mdl-31412917

RESUMEN

BACKGROUND: Lysosomal acid lipase deficiency (LAL-D) is an autosomal recessive disorder that can present as a severe, infantile form also known as Wolman disease. We sought to determine the outcomes and clinical needs of infants diagnosed with LAL-D, treated with enzyme replacement therapy (ERT). METHODS: A chart review was conducted on two infantile-onset LAL-D patients to determine clinical outcomes based on laboratory results, abdominal imaging, growth and dietary records, cardiology, endocrinology, ophthalmology, hematology, and neurocognitive evaluations. RESULTS: Two patients, both diagnosed and treated before 6 months old, demonstrated clinical improvement following weekly ERT. They required dosage increases to optimize growth and symptomatology. Both received a formula low in long chain triglycerides and high in medium chain triglycerides, an intervention that allowed significant catch-up growth. Patient 1 required treatment for partial adrenal insufficiency and hypothyroidism. Both patients demonstrated reduction in liver and spleen size and varying degrees of improved liver function. Neither experienced serious adverse reactions to ERT. CONCLUSION: ERT has led to longer and healthier survival of affected infants. It is imperative that dietary interventions and systemic clinical care become integral to the management. Continued evidence of survival and clinical improvement in this population, coupled with available mass spectrometry enzyme assay from dried blood spots, raises the question of this rare and possibly underdiagnosed disorder's candidacy for newborn screening.


Asunto(s)
Terapia de Reemplazo Enzimático/métodos , Enfermedad de Wolman/diagnóstico , Enfermedad de Wolman/tratamiento farmacológico , Aspartato Aminotransferasas/uso terapéutico , Femenino , Humanos , Lactante , Recién Nacido , Masculino , Espectrometría de Masas , Tamizaje Neonatal , Triglicéridos/uso terapéutico , Enfermedad de Wolman/enzimología , Enfermedad de Wolman
2.
J Clin Pharmacol ; 57(10): 1330-1337, 2017 10.
Artículo en Inglés | MEDLINE | ID: mdl-28425095

RESUMEN

The recreational use of various stimulant drugs has been implicated in the development of movement disorders through dysregulation of the dopaminergic and serotoninergic neurotransmitter systems. The present study investigated psychomotor differences in current and former recreational stimulant drug users compared with nonusing controls. Sixty participants comprised 3 groups: 20 current stimulant drug users (CSUs; 11 men, aged 31.4 ± 9.1 years), 20 former stimulant drug users (FSUs; 5 men, aged 39.1 ± 8.5 years), and 20 nonuser controls (NUCs; 5 men, aged 35.7 ± 6.4 years). Psychomotor arm steadiness for each participant was assessed with a wrist-attached accelerometer during 5 arm positions with eyes open and then eyes closed. Arm-drop of arm position was indicated by the arm longitudinal rotation axis (ALoRA), and tremor was indicated by the overall vector of dynamic body acceleration (VeDBA). Overall, CSUs performed the most poorly on ALoRA (P < .05) and VeDBA indices (P < .05), and FSUs perform almost as poorly on VeDBA indices (P < .05) compared with NUCs. It was concluded that stimulant drug use, primarily MDMA and amphetamines, may result in acute stimulant-induced tremor as well as long-term proprioceptive deficits in terms of arm-droop.


Asunto(s)
Estimulantes del Sistema Nervioso Central/efectos adversos , Trastornos Relacionados con Sustancias/etiología , Temblor/inducido químicamente , Acelerometría , Adulto , Anfetamina/efectos adversos , Brazo/fisiopatología , Consumidores de Drogas , Femenino , Humanos , Masculino , Persona de Mediana Edad , N-Metil-3,4-metilenodioxianfetamina/efectos adversos , Trastornos Relacionados con Sustancias/fisiopatología , Temblor/fisiopatología , Adulto Joven
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