نتایج جستجو برای: neurometabolic disorders

تعداد نتایج: 671446  

2015
Mahmoudreza ASHRAFI Alireza TAVASOLI Omid ARYANI Mohammad VAFAEE-SHAHI

Introduction Canavan disease (CD) is a type of vacuolating leukodystrophy with autosomal recessive inheritance (1). This neurodegenerative disorder is caused by a defect in the aspartoacylase (ASPA) gene encoding the critical enzyme aspartoacylase, which has the role of hydrolyzing N-acetyl-L-aspartic acid (NAA) and providing the acetyl group to oligodendrocytes for myelin synthesis (2, 3). Asp...

2014
J. Ng S. J. R. Heales M. A. Kurian

Childhood neurotransmitter disorders are increasingly recognised as an expanding group of inherited neurometabolic syndromes. They are caused by disturbance in synthesis, metabolism, and homeostasis of the monoamine neurotransmitters, including the catecholamines (dopamine, norepinephrine, and epinephrine) and serotonin. Disturbances in monoamine neurotransmission will lead to neurological symp...

Journal: :The Turkish journal of pediatrics 2012
Göknur Haliloğlu Emine Vezir Leyla Baydar Saniye Onol Serap Sivri Turgay Coşkun Meral Topçu

Neurometabolic diseases diagnosed by cerebrospinal fluid (CSF) examination are GLUT1 deficiency, serine-deficiency syndromes, glycine encephalopathy, cerebral folate deficiency, neonatal vitamin-responsive epileptic encephalopathies, disorders of monoamine metabolism, and y-amino butyric acid (GABA) metabolism. We retrospectively analyzed and compared the demographic, clinical, laboratory, and ...

2017
Tessa Wassenberg Marta Molero-Luis Kathrin Jeltsch Georg F. Hoffmann Birgit Assmann Nenad Blau Angeles Garcia-Cazorla Rafael Artuch Roser Pons Toni S. Pearson Vincenco Leuzzi Mario Mastrangelo Phillip L. Pearl Wang Tso Lee Manju A. Kurian Simon Heales Lisa Flint Marcel Verbeek Michèl Willemsen Thomas Opladen

Aromatic L-amino acid decarboxylase deficiency (AADCD) is a rare, autosomal recessive neurometabolic disorder that leads to a severe combined deficiency of serotonin, dopamine, norepinephrine and epinephrine. Onset is early in life, and key clinical symptoms are hypotonia, movement disorders (oculogyric crisis, dystonia, and hypokinesia), developmental delay, and autonomic symptoms.In this cons...

Journal: :Neurology 2016
Kevin Rostasy Barbara Bajer-Kornek Sunita Venkateswaran Cheryl Hemingway Marc Tardieu

Major advances have been made in the clinical and radiologic characterization of children presenting with the different forms of an acquired inflammatory demyelinating syndrome (ADS) such as acute disseminating encephalomyelitis, neuromyelitis optica spectrum disorders, and clinically isolated syndromes. Nevertheless, a proportion of cases that present with similar symptoms are due to a broad s...

2015
Cátia F. Lourenço Ana Ledo Cândida Dias Rui M. Barbosa João Laranjinha

The functional and structural integrity of the brain requires local adjustment of blood flow and regulated delivery of metabolic substrates to meet the metabolic demands imposed by neuronal activation. This process-neurovascular coupling-and ensued alterations of glucose and oxygen metabolism-neurometabolic coupling-are accomplished by concerted communication between neural and vascular cells. ...

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