Literature DB >> 11383558

Inborn errors of metabolism: a cause of abnormal brain development.

A Nissenkorn1, M Michelson, B Ben-Zeev, T Lerman-Sagie.   

Abstract

Brain malformations are caused by a disruption in the sequence of normal development by various environmental or genetic factors. By modifying the intrauterine milieu, inborn errors of metabolism may cause brain dysgenesis. However, this association is typically described in single case reports. The authors review the relationship between brain dysgenesis and specific inborn errors of metabolism. Peroxisomal disorders and fatty acid oxidation defects can produce migration defects. Pyruvate dehydrogenase deficiency, nonketotic hyperglycinemia, and maternal phenylketonuria preferentially cause a dysgenetic corpus callosum. Abnormal metabolism of folic acid causes neural tube defects, whereas defects in cholesterol metabolism may produce holoprosencephaly. Various mechanisms have been proposed to explain abnormal brain development in inborn errors of metabolism: production of a toxic or energy-deficient intrauterine milieu, modification of the content and function of membranes, or disturbance of the normal expression of intrauterine genes responsible for morphogenesis. The recognition of a metabolic disorder as the cause of the brain malformation has implications for both the care of the patient and for genetic counseling to prevent recurrence in subsequent pregnancies.

Entities:  

Mesh:

Year:  2001        PMID: 11383558     DOI: 10.1212/wnl.56.10.1265

Source DB:  PubMed          Journal:  Neurology        ISSN: 0028-3878            Impact factor:   9.910


  15 in total

1.  Screening for genetic disorders.

Authors:  Nicole Philip
Journal:  Childs Nerv Syst       Date:  2003-06-14       Impact factor: 1.475

2.  A novel homozygous MCOLN1 double mutant allele leading to TRP channel domain ablation underlies Mucolipidosis IV in an Italian Child.

Authors:  Marisol Mirabelli-Badenier; Mariasavina Severino; Barbara Tappino; Domenico Tortora; Francesca Camia; Clelia Zanaboni; Fabia Brera; Enrico Priolo; Andrea Rossi; Roberta Biancheri; Maja Di Rocco; Mirella Filocamo
Journal:  Metab Brain Dis       Date:  2014-08-26       Impact factor: 3.584

3.  Mitochondrial Factors and VACTERL Association-Related Congenital Malformations.

Authors:  S Siebel; B D Solomon
Journal:  Mol Syndromol       Date:  2013-02

4.  Thiamine Deficiency-Mediated Brain Mitochondrial Pathology in Alaskan Huskies with Mutation in SLC19A3.1.

Authors:  Karen Vernau; Eleonora Napoli; Sarah Wong; Catherine Ross-Inta; Jessie Cameron; Danika Bannasch; Andrew Bollen; Peter Dickinson; Cecilia Giulivi
Journal:  Brain Pathol       Date:  2014-10-29       Impact factor: 6.508

Review 5.  Mucolipidosis type IV: an update.

Authors:  Kazuyo Wakabayashi; Ann Marie Gustafson; Ellen Sidransky; Ehud Goldin
Journal:  Mol Genet Metab       Date:  2011-06-16       Impact factor: 4.797

6.  Altered zinc transport disrupts mitochondrial protein processing/import in fragile X-associated tremor/ataxia syndrome.

Authors:  Eleonora Napoli; Catherine Ross-Inta; Sarah Wong; Alicja Omanska-Klusek; Cedrick Barrow; Christine Iwahashi; Dolores Garcia-Arocena; Danielle Sakaguchi; Elizabeth Berry-Kravis; Randi Hagerman; Paul J Hagerman; Cecilia Giulivi
Journal:  Hum Mol Genet       Date:  2011-05-10       Impact factor: 6.150

7.  In vivo pyruvate detected by MR spectroscopy in neonatal pyruvate dehydrogenase deficiency.

Authors:  Dina J Zand; Erin M Simon; Steven B Pulitzer; D J Wang; Z J Wang; Lucy B Rorke; Michael Palmieri; Gerard T Berry
Journal:  AJNR Am J Neuroradiol       Date:  2003-08       Impact factor: 3.825

8.  Radio-imaging for detecting congenitally defective metabolic pathways: A review.

Authors:  Sushil Kachewar; Devidas Kulkarni; Smita Sankaye
Journal:  Australas Med J       Date:  2011-09-30

9.  Co-administration of creatine plus pyruvate prevents the effects of phenylalanine administration to female rats during pregnancy and lactation on enzymes activity of energy metabolism in cerebral cortex and hippocampus of the offspring.

Authors:  Vanessa Trindade Bortoluzzi; Itiane Diehl de Franceschi; Elenara Rieger; Clóvis Milton Duval Wannmacher
Journal:  Neurochem Res       Date:  2014-06-11       Impact factor: 3.996

10.  The Association between EEG Abnormality and Behavioral Disorder: Developmental Delay in Phenylketonuria.

Authors:  Parvaneh Karimzadeh; Mohammad Reza Alaee; Hadi Zarafshan
Journal:  ISRN Pediatr       Date:  2012-03-29
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.