Visit Metagene.de!
Summary
FEEDING: MELAMINE-FORMULA DD
The number of children admitted to hospital in China after drinking infant formula tainted with melamine has risen to 29, 000 [Chen JS 2009], with 104 seriously ill
Although there are a number of articles about nephrotoxicity of melamine (...) melamine can perturb the central nervous system (CNS) function and induce cognitive deficits [An L 2017]
symptoms
cognitive impairment
onset, infancy
renal failure, acute/chronic
urolithiasis, kidney stones
laboratory finding
melamine, ammeline, ammelide, cyanuric acid (MARC) increasedkidney tissue
melamine increasedurine
Literature
Balasubramaniam S,et al.Heterozygous Monocarboxylate Transporter 1 (MCT1, SLC16A1) Deficiency as a Cause of Recurrent KetoacidosisJIMD Rep29033-382015
van Hasselt PM,et al.Monocarboxylate transporter 1 deficiency and ketone utilizationN Engl J Med371201900-19072014
Fingerhut R,et al.Manifestation einer Glutarazidurie Typ I (GA-I) bei einem Kind mit falsch negativem Neugeborenen-Screening31- Jahrestagung APS Fulda 2017002017
Spychala JKitajewski JWnt and beta-catenin signaling target the expression of ecto-5-nucleotidase and increase extracellular adenosine generationExp Cell Res296299-1082004
Sass JOet al.Mutations in ACY1, the Gene Encoding Aminoacylase 1, Cause a Novel Inborn Error of MetabolismAm J Hum Genet783401-4092006
Bashford JA,Chowdhury FA, Shaw CERemarkable motor recovery after riboflavin therapy in adult-onset Brown-Vialetto-Van Laere syndromePract Neurol17153-562017
Juranek IOn augmentation of adenosine-mediated negative dromotropic effect by K+ released during myocardial ischemiaCent Eur J Public Health12033-362004
Marten LM,et al.Kardiomyopathie - ein Symptom des Molybd+ñn-Co-Faktor-Mangels?31. Jahrestagung APS Fulda 2017002017
Chenouard A,et al.A Cause of Permanent Ketosis: GLUT-1 DeficiencyJIMD Rep18079-832015
Lean CB,Lee EJGenetic variations in the MCT1 (SLC16A1) gene in the Chinese population of SingaporeDrug Metab Pharmacokinet245469-4742009
Allison T,et al.Brown-Vialetto-Van Laere Syndrome as a Mimic of Neuroimmune DisordersJ Child Neurol326528-5322017
Peter MCongenital adrenal hyperplasia: 11beta-hydroxylase deficiency.Semin Reprod Med. 2002 Aug20(3):249-54.203249-2542002
Tsiakis K,et al.MONOCARBOXYLATE TRANSPORTER (MCT1)- DEFIZIENZ: Kasuistik +€ber eine neue Ketonk+Ârperverwertungsst+ÂrungAPS Fulda 2017002017
Zaki MS,et al.Molybdenum cofactor and isolated sulphite oxidase deficiencies: Clinical and molecular spectrum among Egyptian patientsEur J Paediatr Neurol205714-7222016
Udhayabanu T,et al.SLC52A2 p.P141T and SLC52A3 p.N21S causing Brown-Vialetto-Van Laere Syndrome in an Indian patient: First genetically proven case with mutations in two riboflavin transportersClin Chim Acta4620210-2142016