Adrenal insufficiency in association with congenital nephrotic syndrome: a case report
-
Isabela Leite Pezzuti
,
Cristiano Túlio Maciel Albuquerque
Abstract
Adrenal disorders in patients with congenital nephrotic syndrome (CNS) have seldom been reported, and the mechanisms that could explain this association are not known. The follow-up of a male infant diagnosed with CNS and primary adrenal insufficiency in his first year of life is the object of this paper.
References
1. Niaudet P. [Congenital and infantile nephrotic syndrome]. Nephrol Ther 2005;1:63–70.10.1016/j.nephro.2005.03.001Search in Google Scholar PubMed
2. Indumathi CK, Dinakar C, Lewin S, Phadke KD. Congenital nephrotic syndrome with adrenal calcification and cardiac malformation. Indian J Pediatr 2005;72: 1049–51.10.1007/BF02724410Search in Google Scholar PubMed
3. Powers RJ, Cohen ML, Williams J. Adrenal calcification in congenital nephrotic syndrome in three American Indians. Pediatr Nephrol 1990;4:29–31.10.1007/BF00858433Search in Google Scholar PubMed
4. Warady BA, Howard CP, Hllerstcin S, Alon U, Grunt JA. Congenital nephrosis in association with hypothyroidism and hypoadrenocorticism. Pediatr Nephrol 1993;7:79–80.10.1007/BF00861580Search in Google Scholar PubMed
5. Brennan A, O’Connor KA, Plant WD, O’Halloran DJ. Nephrotic syndrome: cause of an abnormal response to the rapid ACTH stimulation test. Nephrol Dial Transplant 2004;19:477–8.10.1093/ndt/gfg491Search in Google Scholar PubMed
6. Aso K, Isawa M, Higuchi A, Kotoh S, Hasegawa Y. Stress doses of glucocorticoids cannot prevent progression of all adrenal crises. Clin Pediatr Endocrinol 2009;18:23–7.10.1297/cpe.18.23Search in Google Scholar PubMed PubMed Central
©2014 by Walter de Gruyter Berlin/Boston
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Articles in the same Issue
- Frontmatter
- Original articles
- Assessment of hearing in children with type 1 diabetes mellitus
- Insulin resistance and lipid profiles in HIV-infected Thai children receiving lopinavir/ritonavir-based highly active antiretroviral therapy
- Increased hunger and speed of eating in obese children and adolescents
- Glucagon and insulin cord blood levels in very preterm, late preterm and full-term infants
- Thyroid function in late preterm infants in relation to mode of delivery and respiratory support
- Prevalence of vitamin D deficiency and its related factors in children and adolescents living in North Khorasan, Iran
- Asymmetric dimethyl L-arginine, nitric oxide and cardiovascular disease in adolescent type 1 diabetics
- A combined nutritional-behavioral-physical activity intervention for the treatment of childhood obesity – a 7-year summary
- The effect of earlier puberty on cardiometabolic risk factors in Afro-Caribbean children
- Prevalence of risk of deficiency and inadequacy of 25-hydroxyvitamin D in US children: NHANES 2003–2006
- Serum uric acid: relationships with biomarkers in adolescents and changes over 1 year
- Psychological impact on parents of children with congenital adrenal hyperplasia: a study from Sri Lanka
- Investigation of adropin and leptin levels in pediatric obesity-related nonalcoholic fatty liver disease
- Diseases accompanying congenital hypothyroidism
- Molecular diagnosis of a Chinese pedigree with α-mannosidosis and identification of a novel missense mutation
- Are the characteristics of thyroid cancer different in young patients?
- Unsaturated fatty acids and insulin resistance in childhood obesity
- Effect of genetic subtypes and growth hormone treatment on bone mineral density in Prader-Willi syndrome
- KCNJ11 gene mutation analysis on nine Chinese patients with type 1B diabetes diagnosed before 3 years of age
- Prevalence and risk factors of metabolic syndrome in school adolescents of northeast China
- Patient reports
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- Endocrinological anomalies in a patient with 12q14 microdeletion syndrome. Completing phenotype of this exceptional short stature condition
- Acute mental status change as the presenting feature of adrenal insufficiency in a patient with autoimmune polyglandular syndrome type II and stroke
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- Absence of WNT4 gene mutation in a patient with MURCS association
- Identification of a novel insulin receptor gene heterozygous mutation in a patient with type A insulin resistance syndrome
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- Diabetic lipemia presenting as eruptive xanthomas in a child with autoimmune polyglandular syndrome type IIIa
- A case report of nephrogenic diabetes insipidus with idiopathic Fanconi syndrome in a child who presented with vitamin D resistant rickets
- Letter to the Editor
- Hyperbilirubinemia in neonates of diabetic mothers: an indirect biomarker of organ damage?
