Cargando…
Case report: rare skeletal manifestations in a child with primary hyperparathyroidism
BACKGROUND: Primary hyperparathyroidism (PHPT) is uncommon among children with an incidence of 1:300,000. This diagnosis is often missed in children in contrast to adults where it is detected at a pre symptomatic stage due to routine blood investigations. Etiology of PHPT can be due to adenoma, hype...
Autores principales: | Arambewela, Maulee Hiromi, Liyanarachchi, Kamani Danushka, Somasundaram, Noel P., Pallewatte, Aruna S., Punchihewa, Gamini L. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5521059/ https://www.ncbi.nlm.nih.gov/pubmed/28732535 http://dx.doi.org/10.1186/s12902-017-0197-z |
Ejemplares similares
-
Extreme hypernatremia as a probable cause of fatal arrhythmia: a case report
por: Arambewela, Maulee Hiromi, et al.
Publicado: (2016) -
Primary hyperparathyroidism in pregnancy: experience of a tertiary centre
por: Arshad, Muhammad Fahad, et al.
Publicado: (2022) -
Prevalence of Depression and Associated Factors among Patients with Type 2 Diabetes Attending the Diabetic Clinic at a Tertiary Care Hospital in Sri Lanka: A Descriptive Study
por: Arambewela, Maulee Hiromi, et al.
Publicado: (2019) -
Rare Skeletal Complications in the Setting of Primary Hyperparathyroidism
por: Sabanis, Nikos, et al.
Publicado: (2015) -
Renal manifestations of primary hyperparathyroidism
por: Lila, Anurag Ranjan, et al.
Publicado: (2012)