Cargando…
Genetic testing can change diagnosis and treatment in children with congenital hypothyroidism
OBJECTIVE: Guidelines on congenital hypothyroidism (CH) recommend that genetic testing should aim to improve diagnosis, treatment or prognosis, but it is unclear which patients would benefit most from the genetic investigation. We aimed to investigate the genetic etiology of transient CH (TCH) and p...
Autores principales: | Kara, Cengiz, Mammadova, Jamala, Abur, Ümmet, Gumuskaptan, Cagri, İzci Güllü, Elif, Dağdemir, Ayhan, Aydın, Murat |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Bioscientifica Ltd
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10160543/ https://www.ncbi.nlm.nih.gov/pubmed/36913313 http://dx.doi.org/10.1530/ETJ-22-0212 |
Ejemplares similares
-
Nephrogenic Syndrome of Inappropriate Antidiuresis Mimicking Hyporeninemic Hypoaldosteronism: Case Report of Two Infants
por: Mammadova, Jamala, et al.
Publicado: (2023) -
Evaluation of the promoter methylation status of hypoxia factor 3A and interleukin-6 genes and expression levels of mir-130b and mir-146b in childhood obesity
por: Tekcan, Esra, et al.
Publicado: (2022) -
Transient Congenital Hypothyroidism in Turkey: An Analysis on Frequency and Natural Course
por: Kara, Cengiz, et al.
Publicado: (2016) -
Congenital Goitrous Hypothyroidism, Deafness and Iodide Organification Defect in Four Siblings: Pendred or Pseudo−Pendred Syndrome?
por: Kara, Cengiz, et al.
Publicado: (2010) -
Frequency of obesity and metabolic syndrome in childhood leukemia and lymphoma survivors
por: Kartal, İbrahim, et al.
Publicado: (2022)