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1.
Pediatr Nephrol ; 37(7): 1623-1646, 2022 07.
Artigo em Inglês | MEDLINE | ID: mdl-34993602

RESUMO

BACKGROUND: Genetic kidney diseases contribute a significant portion of kidney diseases in children and young adults. Nephrogenetics is a rapidly evolving subspecialty; however, in the clinical setting, increased use of genetic testing poses implementation challenges. Consequently, we established a national nephrogenetics clinic to apply a multidisciplinary model. METHODS: Patients were referred from different pediatric or adult nephrology units across the country if their primary nephrologist suspected an undiagnosed genetic kidney disease. We determined the diagnostic rate and observed the effect of diagnosis on medical care. We also discuss the requirements of a nephrogenetics clinic in terms of logistics, recommended indications for referral, and building a multidisciplinary team. RESULTS: Over 24 months, genetic evaluation was completed for a total of 74 unrelated probands, with an age range of 10 days to 72 years. The most common phenotypes included congenital anomalies of the kidneys and urinary tract, nephrotic syndrome or unexplained proteinuria, nephrocalcinosis/nephrolithiasis, tubulopathies, and unexplained kidney failure. Over 80% of patients were referred due to clinical suspicion of an undetermined underlying genetic diagnosis. A molecular diagnosis was reached in 42/74 probands, yielding a diagnostic rate of 57%. Of these, over 71% of diagnoses were made via next generation sequencing (gene panel or exome sequencing). CONCLUSIONS: We identified a substantial fraction of genetic kidney etiologies among previously undiagnosed individuals which influenced subsequent clinical management. Our results support that nephrogenetics, a rapidly evolving field, may benefit from well-defined multidisciplinary co-management administered by a designated team of nephrologist, geneticist, and bioinformatician. A higher resolution version of the Graphical abstract is available as Supplementary information.


Assuntos
Testes Genéticos , Nefropatias , Criança , Humanos , Nefropatias/genética , Fenótipo , Encaminhamento e Consulta , Sequenciamento do Exoma/métodos
2.
Harefuah ; 160(12): 810-813, 2021 Dec.
Artigo em Hebraico | MEDLINE | ID: mdl-34957717

RESUMO

INTRODUCTION: The rising popularity of hair straightening in younger ages has become a medical issue, since glycolic acid and formaldehyde may be present, even in "formaldehyde-free" labeled products. Formaldehyde - a colorless material, evaporates during the hair straightening procedure, inhaled and absorbed into the blood stream causing oxidative stress and cytotoxic damage to the proximal tubule cells leading to acute kidney injury (AKI). Glycolic acid is processed to glyoxylate and eventually to oxalate, whose deposition may also cause AKI. We present three cases of female teenagers with AKI, recently after a hair straightening procedures. All patients had features of tubular damage and kidney biopsies in the first 2 cases showed acute tubular necrosis (ATN), one with oxalate deposition and the other with unidentified depositions. Two cases required acute dialysis, and shortly after commencing it, kidney function rapidly improved. We believe that in the presented cases, the prompt dialysis cleared a nephrotoxic ingredient, allowing improvement of renal function, therefore preventing long-standing and maybe, even permanent damage. This case presentation highlights the danger of hair straightening products in pediatric populations aiming to increase its index of suspicion among adult and pediatric nephrologists.


Assuntos
Injúria Renal Aguda , Formaldeído , Adolescente , Feminino , Humanos , Diálise Renal
4.
Pediatr Transplant ; 18(1): 23-8, 2014 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-24134654

RESUMO

Cardiovascular-related mortality is 100-fold higher in pediatric renal transplant recipients than in the age-matched general population. Seventy-seven post-renal transplant children's charts were reviewed for cardiovascular risk factors at two and six months after transplantation (short term) and at two yr after transplantation and the last follow-up visit (mean 7.14 ± 3.5 yr) (long term). Significant reduction was seen in cardiovascular risk factors prevalence from two months after transplantation to last follow-up respectively: Hypertension from 52.1% to 14%, hypercholesterolemia from 48.7% to 33%, hypertriglyceridemia from 50% to 12.5%, anemia from 29.6% to 18.3%, hyperparathyroidism from 32% to 18.3% and hyperglycemia from 11.7% to 10%, and left ventricular hypertrophy from 25.8% at short term to 15%. There was an increase in the prevalence of obesity from 1.5% to 3.9% and of CKD 3-5 from 4.75% to 24%. The need for antihypertensive treatment decreased from 54% to 42%, and the percentage of patients controlled by one medication rose from 26% to 34%, whereas the percentage controlled by 2, 3, and 4 medications decreased from 21.9%, 5.5%, and 1.4% to 6%, 2%, and 0. Children after renal transplantation appear to have high rates of cardiovascular risk factors, mainly on short-term follow-up.


Assuntos
Doenças Cardiovasculares/complicações , Transplante de Rim , Insuficiência Renal/terapia , Adolescente , Adulto , Anemia/complicações , Anti-Hipertensivos/uso terapêutico , Criança , Pré-Escolar , Feminino , Seguimentos , Taxa de Filtração Glomerular , Humanos , Hipercolesterolemia/complicações , Hiperglicemia/complicações , Hiperparatireoidismo/complicações , Hipertensão/complicações , Hipertrigliceridemia/complicações , Hipertrofia Ventricular Esquerda/complicações , Imunossupressores/uso terapêutico , Lactente , Recém-Nascido , Masculino , Obesidade/complicações , Insuficiência Renal/complicações , Estudos Retrospectivos , Fatores de Risco , Fatores de Tempo , Adulto Jovem
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