Asunto(s)
Humanos , Masculino , Femenino , Niño , Síndrome Nefrótico/genética , Mutación , Esteroides/farmacocinética , Resistencia a MedicamentosRESUMEN
In this study, we aimed to analyze features and outcome of convulsion in pediatric lupus nephritis patients. We retrospectively reviewed data of 14 Iranian children with lupus nephritis who developed seizures and compared them with a group of the same number of well matched pediatric lupus nephritis patients. Higher serum creatinine levels and higher frequencies of anemia and lymphopenia were observed in the convulsion group. Multivariable logistic regression analysis revealed that the only risk factor for development of convulsion in pediatric lupus patients with nephritis was lymphopenia. Survival analysis showed that convulsion had no impact on patient and renal function outcomes in our pediatric lupus nephritis subjects. In conclusion, we found that lymphopenia is a predictive factor for convulsion occurrence in our patients and special attention to neurological status assessment may be needed in this situation.
Asunto(s)
Nefritis Lúpica/complicaciones , Linfopenia/complicaciones , Convulsiones/etiología , Adolescente , Anemia/complicaciones , Biomarcadores/sangre , Estudios de Casos y Controles , Niño , Creatinina/sangre , Femenino , Humanos , Irán/epidemiología , Estimación de Kaplan-Meier , Modelos Logísticos , Nefritis Lúpica/sangre , Nefritis Lúpica/mortalidad , Linfopenia/sangre , Masculino , Estudios Retrospectivos , Medición de Riesgo , Factores de Riesgo , Convulsiones/sangre , Convulsiones/mortalidad , Factores de Tiempo , Regulación hacia ArribaAsunto(s)
Nefritis Lúpica/diagnóstico , Nefritis Lúpica/epidemiología , Pericarditis/diagnóstico , Pericarditis/epidemiología , Adolescente , Distribución por Edad , Niño , Preescolar , Comorbilidad , Progresión de la Enfermedad , Quimioterapia Combinada , Femenino , Pruebas de Función Cardíaca , Humanos , Incidencia , Irán/epidemiología , Estimación de Kaplan-Meier , Pruebas de Función Renal , Nefritis Lúpica/tratamiento farmacológico , Masculino , Pericarditis/tratamiento farmacológico , Pronóstico , Modelos de Riesgos Proporcionales , Medición de Riesgo , Índice de Severidad de la Enfermedad , Distribución por Sexo , Análisis de SupervivenciaRESUMEN
Hereditary vitamin D-resistant rickets type or vitamin D-dependent rickets type II is a genetically determined and rare autosomal recessive disorder, most often caused by mutations in the vitamin D receptor gene. It usually presents with rachitic changes not responsive to vitamin D treatment and the circulating levels of 1,25 (OH)2 vitamin D-3 are elevated, differentiating it from vitamin D-dependent rickets type I. Alopecia capitis or alopecia totalis is seen in some families with vitamin D-dependent rickets type II. This is usually associated with a more severe phenotype. In this report, we present the clinical findings on a family which exhibited the typical clinical features of hereditary vitamin D-resistant rickets in two siblings. In addition, molecular analysis of the vitamin D receptor gene was performed by sequencing all coding exons. The cardinal findings in the index patient were alopecia totalis, renal tubular acidosis, mild generalized aminoaciduria, refractory rickets, high alkaline phosphatase, and hyperparathyroidism. Other routine biochemical tests were within normal limits, but 1+ glycine was detected in his urine. Skin biopsy results were compatible with alopecia areata. A previous child with similar phenotype was reported to be deceased at the age of 32 months. Mutation analysis of the vitamin D receptor gene by direct sequencing analysis of all coding exons showed a homozygous c.122GA(p.Cys41Tyr) variant in exon 2 with several arguments pointing to a pathogenic effect. We should be aware of this very rare disease whenever we see a patient with refractory rickets and alopecia.