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临床试验/DRKS00007878
DRKS00007878招募中不适用

iNTD (International Network on Neurotransmitter related Disorders) Registry - iNTD

niversitätsklinikum Heidelberg0 个研究点目标入组 500 人开始时间: 2015年3月6日最近更新:

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
500

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

年龄范围
one 至 one(—)
性别
All

入选标准

  • Children and adults with confirmed diagnosis of Neurotransmitter (biogenic amines) disorders
  • o Aromatic amino acid decarboxylase (AADC) deficiency
  • o Tyrosine hydroxylase (TH) deficiency
  • o Dopamine beta-hydroxylase (DßH) deficiency
  • o Monoamine oxidase A (MAOA) deficiency
  • o Dopamine transporter (DAT) deficiency
  • o Vesicular monoamine transporter 2 (VMAT) deficiency
  • Children and adults with confirmed diagnosis of BH4 Deficiencies
  • o Autosomal rezessive GTP cyclohydrolase deficiency
  • o Autosomal dominant GTP cyclohydrolase deficiency (Segawa disease)
  • o 6-Pyruvoyl-tetrahydropterin synthase (PTPS) deficiency
  • o Dihydropteridine reductase (DHPR) deficiency
  • o Sepiapterin reductase (SR) deficiency
  • o Pterin-4a-carbinolamine dehydratase (PCD) deficiency
  • Children and adults with confirmed diagnosis of cerebral folate deficiencies:
  • o Folate receptor alpha (FOLR1) deficiency
  • o Dihydrofolate reductase (DHFR) deficiency
  • Children and adults with confirmed diagnosis of serine deficiency disorders:
  • o 3-phosphoglycerate dehydrogenase (3-PGDH) deficiency
  • o 3-phosphoserine phosphatase (3-PSP) deficiency
  • o Phosphoserine aminotransferase deficiency
  • Children and adults with confirmed diagnosis of disorders of glycine metabolism:
  • o Glycine encephalopathy (Non-ketotic hyperglycinaemia)
  • Children and adults with confirmed diagnosis of GABA related disorders
  • o GABA-transaminase-deficiency
  • o Succinate-semialdehyde-dehydroxylase deficiency
  • Children and adults with suspicious CSF results (suggesting neurotransmitter related disorder) without known diagnosis
  • Written informed consent given by the patient, the parents or the legal representatives

排除标准

  • Individuals with rare and unrelated serious comorbidities:
  • o Down Syndrome
  • o Intraventricular haemorrhage (°III-IV)
  • o Severe hyperbilirubinemia with Kernikterus,
  • o Embryo fetal alcohol syndrome
  • o Intake of teratogen drugs during pregnancy

研究者

发起方
niversitätsklinikum Heidelberg

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