Literature DB >> 15884622

Maple syrup urine disease-treatment and outcome in patients of Turkish descent in Germany.

Eva Simon1, Udo Wendel, Peter Schadewaldt.   

Abstract

Maple syrup urine disease (MSUD) is a rare autosomal recessive disorder that causes acute and chronic brain dysfunction because of a neurotoxic effect of the accumulating branched chain amino acids (BCAA) and their corresponding keto acids. Aim of the treatment is a rapid reversal of the neonatal decompensation and a stable long-term metabolic control obtained by a carefully adjusted BCAA-low diet. In optimally treated patients, an unimpaired neurological and intellectual outcome is possible. Ten patients of Turkish origin suffering from MSUD are presently treated in the Metabolic Unit of the University Hospital in Düsseldorf, Germany. All patients show mild intellectual deficits; neurological impairment is rare. This paper aims to define the feasible standard of therapy and the resulting intellectual and psychosocial outcome achievable in MSUD patients of Turkish origin under high standard conditions of medical care for inborn errors of metabolism.

Entities:  

Mesh:

Substances:

Year:  2005        PMID: 15884622

Source DB:  PubMed          Journal:  Turk J Pediatr        ISSN: 0041-4301            Impact factor:   0.552


  5 in total

1.  Liver transplantation for classical maple syrup urine disease: long-term follow-up in 37 patients and comparative United Network for Organ Sharing experience.

Authors:  George V Mazariegos; D Holmes Morton; Rakesh Sindhi; Kyle Soltys; Navdeep Nayyar; Geoffrey Bond; Diana Shellmer; Benjamin Shneider; Jerry Vockley; Kevin A Strauss
Journal:  J Pediatr       Date:  2011-08-11       Impact factor: 4.406

2.  Classical maple syrup urine disease and brain development: principles of management and formula design.

Authors:  Kevin A Strauss; Bridget Wardley; Donna Robinson; Christine Hendrickson; Nicholas L Rider; Erik G Puffenberger; Diana Shellmer; Diana Shelmer; Ann B Moser; D Holmes Morton
Journal:  Mol Genet Metab       Date:  2010-01-12       Impact factor: 4.797

3.  Prenatal diagnosis of a novel mutation, c.529C>T (p.Q177X), in the BCKDHA gene in a family with maple syrup urine disease.

Authors:  R Tammachote; S Tongkobpetch; T Desudchit; K Suphapeetiporn; V Shotelersuk
Journal:  J Inherit Metab Dis       Date:  2009-02-24       Impact factor: 4.982

4.  Plasma amino acid and urine organic acid profiles of Filipino patients with maple syrup urine disease (MSUD) and correlation with their neurologic features.

Authors:  Mary Anne D Chiong; Marilyn A Tan; Cynthia P Cordero; Esphie Grace D Fodra; Judy S Manliguis; Cristine P Lopez; Leslie Michelle M Dalmacio
Journal:  Mol Genet Metab Rep       Date:  2016-10-12

5.  Oral health status of children and young adults with maple syrup urine disease in Turkey.

Authors:  Elif Ballikaya; Yılmaz Yildiz; Nagihan Koç; Ayşegül Tokatli; Meryem Uzamis Tekcicek; Hatice Serap Sivri
Journal:  BMC Oral Health       Date:  2021-01-06       Impact factor: 2.757

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.