adrenoleukodystrophy : Related Words Words similar in meaning to adrenoleukodystrophy
- adrenomyeloneuropathy«
- nerve cell«
- ald«
- myelin«
- vlcfa«
- genetic«
- adrenal insufficiency«
- disease«
- degenerative«
- gene therapy«
- brain«
- childhood cerebral form«
- abcd1 mutation«
- lorenzo«
- symptom«
- loes score«
- demyelination process«
- ald patient«
- abcd1«
- chain fatty acid«
- incidence«
- mutation«
- patient«
- plasma«
- dietary therapy«
- phenotype«
- transplant«
- male«
- cerebral form«
- ald phenotype«
- oil«
- treatment«
- cerotic acid«
- phenotype correlation«
- adrenal function«
- dietary treatment«
- body«
- female carrier«
- recessive inheritance«
- hormone replacement«
- leydig cell«
- stem cell transplant«
- demyelination«
- adrenal cortex«
- neurological symptom«
- progression«
- clinical presentation«
- hyperactivity«
- body tissue«
- tissue«
- x chromosome«
- gene«
- genotype«
- testis«
- pathogenesis«
- form«
- wild type abcd1«
- vlcfa level«
- vlcfa concentration«
- unsaturated vlcfa«
- traditional transplant«
- siemerling–creutzfeldt disease«
- progressive demyelination«
- positive plasma vlcfa determination«
- plasma vlcfa measurement«
- plasma vlcfa level«
- peroxisomal membrane transporter protein«
- peroxisomal membrane transporter«
- peroxisomal fatty acid beta oxidation«
- normal vlcfa«
- neuroradiologist daniel j. loes md«
- male adrenoleukodystrophy phenotypes«
- heterozygote female«
- glycerol trioleate«
- gene abcd1«
- female adrenoleukodystrophy phenotypes«
- fatty acid buildup«
- excess vlcfa«
- eventual phenotype«
- common peroxisomal inborn error«
- common male phenotype«
- chain fatty acid concentration«
- cerebral childhood form«
- cerebral ald«
- bronze schilder disease«
- appropriate vector«
- adrenomyeloneuropathy presentation«
- universal newborn screening«
- progressive paraparesis«
- overall incidence«
- glyceryl trierucate«
- chain fatty acid substrate«
- individual«
- level«
- characteristic elevation«
- relevant enzyme«
- neurological degradation«
- myelin sheathes«
- hla match«
- cerebral manifestation«
- biochemical phenotype«
- accumulation«
- hemizygous male«
- germline mosaicism«
- rapid degeneration«
- multiple phenotype«
- endogenous synthesis«
- carrier parent«
- frame deletion«
- heterogeneous disorder«
- lorenzo odone«
- biochemically«
- carrier female«
- family«
- paraparesis«
- single x chromosome«
- frameshifts«
- distinct phenotype«
- disorder«
- older patient«
- hematopoietic stem cell transplant«
- onset«
- successful transplant«
- newborn screening program«
- causative mutation«
- severe manifestation«
- diagnosis difficult«
- cell transplant«
- clinical severity«
- molecular genetic analysis«
- boy«
- usuhs«
- clinical phenotype«
- effectiveness«
- muscle stiffness«
- disease phenotype«
- synthetic pathway«
- clinical suspicion«
- symptomatic patient«
- saturated fatty acid«
- verbal instruction«
- peroxisomes«
- common mutation«
- presentation«
- emotional instability«
- disruptive behavior«
- procedure«
- carbon chain«
- dietary intake«
- unsaturated fatty acid«
- dietary restriction«
- initial symptom«
- varied collection«
- missense mutation«
- clinically«
- affected individual«
- mri.«
- similar procedure«
- initial testing«
- pattern«
- disease progression«
- biotechnology information«
- white matter«
- gas chromatography«
- clinical symptom«
- sexual dysfunction«
- successful treatment«
- normal development«
- specific country«
- supplementation«
- atrophy«
- bone marrow transplant«
- similar symptom«
- difficulty«
- exact mechanism«
- molecular analysis«
- severe form«
- significant risk«
- elongation«
- genetics«
- initial attempt«
- treatment option«
- mass spectrometry«
- bone marrow«
- speaking«
- presence«
- female«
- localization«
- abnormality«
- adult male«
- central nervous system«
- diagnosis«
- effort«
- intake«
- variety«
- metabolism«
- hallmark«
- system«
- syndrome«
- degradation«
- defect«
- national center«
- nerve«
- severity«
- realization«
