Cargando…
The first Turkish family with Rotor syndrome diagnosed at the molecular level
Rotor syndrome is defined as a self-limiting hyperbilirubinemia characterized by jaundice that does not need treatment, cause any morbidity or affect life expectancy. As far as the literature is evaluated, the number of patients with Rotor syndrome diagnosed at the molecular level is less than 20 un...
Autores principales: | Gümüş, Evren, Karaca, Meryem, Deveci, Uğur, Jirsa, Milan |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Kare Publishing
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7750336/ https://www.ncbi.nlm.nih.gov/pubmed/33414662 http://dx.doi.org/10.14744/TurkPediatriArs.2019.55798 |
Ejemplares similares
-
Clinical characteristics of a Turkish family with congenital erythrocytosis due to an EPOR mutation: Is routine phlebotomy indicated in children and adolescents?
por: Sarper, Nazan, et al.
Publicado: (2020) -
SLC26A3 mutation in Turkish neonate and her sibling with congenital chloride diarrhea
por: Doğan, Erkan, et al.
Publicado: (2020) -
Recurrent infections, neurologic signs, low serum uric acid levels, and lymphopenia in childhood: Purine nucleoside phosphorylase deficiency, an emergency for infants
por: Kütükçüler, Necil, et al.
Publicado: (2020) -
A rare case in childhood: Pott’s puffy tumor developing secondary to frontal sinus osteoma
por: Öztürk, Necmiye, et al.
Publicado: (2020) -
A rare cause of acute severe upper airway obstruction that required endotracheal intubation: adenoid hypertrophy
por: Yıldırım, Uğur, et al.
Publicado: (2020)