نتایج جستجو برای: neonatal hypoglycemia

تعداد نتایج: 93267  

2016
Kyoungmin Kim Johanna Inhyang Kim Bung-Nyun Kim Jae-Won Kim Soon-beom Hong Soo-Chul Cho

Objective: The objective of this study was to investigate the characteristics of language profiles according to whether or not Korean children with autism spectrum disorder (ASD) also have ADHD, and to examine the relationship with executive function. Methods: Participants in the study were boys with ADHD aged 6 to 11 years who visited the clinic from January 2012 to December 2013. In this stud...

2015
Alina Grama Oana Marginean Iulian Velea Corina Paul Mihaela Chincesan Lorena Elena Melit

Introduction. Hypoglycemia with its diverse causes is frequently encountered in the pediatrics pathology, beginning with the neonatal period and until the adolescent one. Through its consequences, both, the early (seizures, coma) and the late ones (neurological impairment), hypoglycemia must be identifi ed, prevented, avoided and treated. Objectives. To present the clinical evolution of a femal...

Journal: :PANACEA JOURNAL OF MEDICAL SCIENCES 2023

Neonatal hypoglycemia is common metabolic disorder. Hyperglycemia can also occur in other conditions like exogenous parenteral glucose administration, preterm, ELBW babies, stressed premature infants (requiring mechanical ventilation), hypoxia or neonatal diabetes mellitus. The major clinical problems associated with hyperglycemia are hyper osmolality and osmotic dieresis leading to alteration ...

Journal: :American Journal of Obstetrics and Gynecology 2018

Journal: :International Journal of Family & Community Medicine 2021

Journal: :Neonatal and Pediatric Medicine 2017

2017
Abdulsalam Abu-Libdeh Bassam Abu-Libdeh Ulla Najwa Abdulhag

Congenital hypopituitarism is a rare condition associated with possible serious complications and long-term neurological sequelae, if not promptly recognized and treated.1 Neonates with congenital hypopituitarism may present with or without associated developmental defects, such as ocular, midline, and genital abnormalities. They may also present with nonspecific symptoms, including hypoglycemi...

Journal: :Pediatrics 2012
Saadet Mercimek-Mahmutoglu Gabriella A Horvath Marion Coulter-Mackie Tanya Nelson Paula J Waters Michael Sargent Eduard Struys Cornelis Jakobs Sylvia Stockler-Ipsiroglu Mary B Connolly

Pyridoxine-dependent epilepsy (PDE) was first described in 1954. The ALDH7A1 gene mutations resulting in α-aminoadipic semialdehyde dehydrogenase deficiency as a cause of PDE was identified only in 2005. Neonatal epileptic encephalopathy is the presenting feature in >50% of patients with classic PDE. We report the case of a 13-month-old girl with profound neonatal hypoglycemia (0.6 mmol/L; refe...

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