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1.
J Pediatr ; 135(4): 494-9, 1999 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-10518084

RESUMEN

OBJECTIVE: To report chronic fatigue syndrome (CFS) associated with both Ehlers-Danlos syndrome (EDS) and orthostatic intolerance. STUDY DESIGN: Case series of adolescents referred to a tertiary clinic for the evaluation of CFS. All subjects had 2-dimensional echocardiography, tests of orthostatic tolerance, and examinations by both a geneticist and an ophthalmologist. RESULTS: Twelve patients (11 female), median age 15.5 years, met diagnostic criteria for CFS and EDS, and all had either postural tachycardia or neurally mediated hypotension in response to orthostatic stress. Six had classical-type EDS and 6 had hypermobile-type EDS. CONCLUSIONS: Among patients with CFS and orthostatic intolerance, a subset also has EDS. We propose that the occurrence of these syndromes together can be attributed to the abnormal connective tissue in dependent blood vessels of those with EDS, which permits veins to distend excessively in response to ordinary hydrostatic pressures. This in turn leads to increased venous pooling and its hemodynamic and symptomatic consequences. These observations suggest that a careful search for hypermobility and connective tissue abnormalities should be part of the evaluation of patients with CFS and orthostatic intolerance syndromes.


Asunto(s)
Síndrome de Ehlers-Danlos/complicaciones , Síndrome de Fatiga Crónica/complicaciones , Hipotensión Ortostática/complicaciones , Adolescente , Adulto , Presión Sanguínea , Niño , Síndrome de Ehlers-Danlos/diagnóstico , Síndrome de Fatiga Crónica/diagnóstico , Femenino , Frecuencia Cardíaca , Humanos , Hipotensión Ortostática/diagnóstico , Masculino
3.
J Pediatr ; 120(6): 934-7, 1992 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-1593355

RESUMEN

We describe a female infant with typical features of the cobalamin C form of combined methylmalonic aciduria and homocystinuria who also had the hemolytic-uremic syndrome with thrombocytopenia, microangiopathic hemolytic anemia, hypertension, and renal failure. Review of this and other described cases of the cobalamin C defect suggests that the hemolytic-uremic syndrome is part of the phenotypic spectrum of this inborn error of cobalamin metabolism.


Asunto(s)
Síndrome Hemolítico-Urémico/complicaciones , Homocistinuria/complicaciones , Errores Innatos del Metabolismo/complicaciones , Ácido Metilmalónico/orina , Vitamina B 12/metabolismo , Femenino , Genes Recesivos , Homocistinuria/genética , Humanos , Recién Nacido , Errores Innatos del Metabolismo/genética , Fenotipo
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