Assessment
Questionnaire

Have a symptom?
See what questions
a doctor would ask.
 
Symptoms » Neurological problems » Glossary
 

Glossary for Neurological problems

Medical terms related to Neurological problems or mentioned in this section include:

  • Absence of septum pellucidum and septo-optic dysplasia: A rare birth defect where a thin membrane in the middle of the brain is missing. This brain abnormality is never present on it's own but is a characteristic of septo-optic dysplasia where the patient also has optic disk abnormalities and pituitary deficiencies.
  • Adducted thumb syndrome recessive form: A rare recessively inherited disorder characterized mainly by a small head, arthrogryposis (joint contractures), cleft palate and various other abnormalities.
  • Adducted thumbs -- arthrogryposis, Christian type: A rare recessively inherited disorder characterized mainly by a small head, arthrogryposis (joint contractures), cleft palate and various other abnormalities.
  • Alopecia: Partial or total loss of hair due to aging, an endocrine disorder, drug reaction, anticancer medication or skin disease.
  • Alopecia, mental retardation and neurological problems: A rare, newly described syndrome characterized by baldness, mental retardation and neurological problems.
  • Arteriovenous Malformation: Birth defect of a tangle of veins and arteries.
  • Atypical hemolytic uremic syndrome: A rare condition characterized by hemolytic anemia, thrombocytopenia and kidney failure that has no obvious cause.
  • Balo disease: A rare neurological disorder where the protective sheath around brain nerve fibres are progressively destroyed. Symptoms are determined by the size and location of the affected brain area.
  • Behavioral symptoms: Symptoms of personal behavior.
  • Braddock Jones Superneau syndrome: A very rare disorder characterized primarily by the premature fusion of skull bones (sagittal), the Dandy-Walker malformation and a buildup of fluid in the brain (hydrocephalus). The Dandy-Walker malformation is where a cyst develops in the back of the brain and interferes with the movement of fluid through the brain resulting in an accumulation of fluid.
  • Brain symptoms: Symptoms affecting the brain
  • Chemical poisoning -- Lead-containing Paint: Lead pain contains lead as well as other harmful chemicals. The lead in the pain is toxic (especially to young children) and ingesting fresh or old paint can cause serious symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the exposure.
  • Chromosome 14 deletion: A rare genetic disorder where deletion genetic material from chromosome 14 causes various abnormalities. The type and severity of symptoms varies depending on the size and location of the genetic material that is deleted.
  • Chromosome 17 deletion: A rare genetic disorder where deletion genetic material from chromosome 17 causes various abnormalities. The type and severity of symptoms varies depending on the size and location of the genetic material that is deleted.
  • Chromosome 17 trisomy: A rare genetic disorder where duplication of genetic material from chromosome 17 causes various abnormalities. The type and severity of symptoms varies depending on the size and location of the genetic material that is duplicated.
  • Cobalamin malabsorption, selective, with proteinuria: A rare inherited disorder characterized by vitamin B12 deficiency which results from the body's inability to absorb vitamin B12 from the foods eaten.
  • Cognitive impairment: General loss of mental or cognitive ability
  • Congenital Vitamin B12 Malabsorption: A rare inherited disorder characterized by vitamin B12 deficiency which results from the body's inability to absorb vitamin B12 from the foods eaten.
  • Craniosynostosis -- Dandy-Walker -- Hydrocephalus: A very rare disorder characterized primarily by the premature fusion of skull bones (sagittal), the Dandy-Walker malformation and a buildup of fluid in the brain (hydrocephalus). The Dandy-Walker malformation is where a cyst develops in the back of the brain and interferes with the movement of fluid through the brain resulting in an accumulation of fluid.
  • Craniosynostosis, sagittal, with Dandy-Walker malformation and hydrocephalus: A very rare disorder characterized primarily by the premature fusion of skull bones (sagittal), the Dandy-Walker malformation and a buildup of fluid in the brain (hydrocephalus). The Dandy-Walker malformation is where a cyst develops in the back of the brain and interferes with the movement of fluid through the brain resulting in an accumulation of fluid.
  • Cystic leukoencephalopathy without megalencephaly: A rare genetic brain disorder characterized by the development of cystic changes in the brain resulting in neurological problems. The condition is nonprogressive.
  • Developmental problems: Physical or mental development difficulty.
  • Familial Selective Vitamin B12 Malabsorption: A rare inherited disorder characterized by vitamin B12 deficiency which results from the body's inability to absorb vitamin B12 from the foods eaten.
  • Fetal Valproate Syndrome: A condition affecting the fetus caused by the medication valproate
  • Graeck-Imerslund disease:
  • Grasbeck-Imerslund Disease: A rare inherited disorder characterized by vitamin B12 deficiency which results from the body's inability to absorb vitamin B12 from the foods eaten.
  • Head symptoms: Symptoms affecting the head or brain
  • Helminthiasis: Infection of the human body with a parasitic worm such as roundworms and pinworms. The worms usually only involve the intestinal tract but sometimes they may invade other organs. The type and severity of symptoms is determined by the type of worm and the part of the body infected.
  • Hemolytic Uremic Syndrome, Atypical, Susceptibility to, 1: Atypical hemolytic uremic syndrome is a rare condition characterized by hemolytic anemia, thrombocytopenia and kidney failure that has no obvious cause. Researchers have discovered a number of genes linked to an increased susceptibility to developing the condition. Type 1 is linked to a genetic defect on chromosome 8q34.3.
  • Hemolytic Uremic Syndrome, Atypical, Susceptibility to, 2: Atypical hemolytic uremic syndrome is a rare condition characterized by hemolytic anemia, thrombocytopenia and kidney failure that has no obvious cause. Researchers have discovered a number of genes linked to an increased susceptibility to developing the condition. Type 2 is linked to a genetic defect on chromosome 1q32.
  • Hemolytic Uremic Syndrome, Atypical, Susceptibility to, 3: Atypical hemolytic uremic syndrome is a rare condition characterized by hemolytic anemia, thrombocytopenia and kidney failure that has no obvious cause. Researchers have discovered a number of genes linked to an increased susceptibility to developing the condition. Type 3 is linked to a genetic defect on chromosome 4q25.
  • Hemolytic Uremic Syndrome, Atypical, Susceptibility to, 4: Atypical hemolytic uremic syndrome is a rare condition characterized by hemolytic anemia, thrombocytopenia and kidney failure that has no obvious cause. Researchers have discovered a number of genes linked to an increased susceptibility to developing the condition. Type 4 is linked to a genetic defect on chromosome 6p21.3.
  • Hemolytic Uremic Syndrome, Atypical, Susceptibility to, 5: Atypical hemolytic uremic syndrome is a rare condition characterized by hemolytic anemia, thrombocytopenia and kidney failure that has no obvious cause. Researchers have discovered a number of genes linked to an increased susceptibility to developing the condition. Type 5 is linked to a genetic defect on chromosome 19p13.3-p13.2.
  • Hemolytic Uremic Syndrome, Atypical, Susceptibility to, 6: Atypical hemolytic uremic syndrome is a rare condition characterized by hemolytic anemia, thrombocytopenia and kidney failure that has no obvious cause. Researchers have discovered a number of genes linked to an increased susceptibility to developing the condition. Type 6 is linked to a genetic defect on chromosome 20p11.2.
  • Imerslund's Anemia: A rare inherited disorder characterized by vitamin B12 deficiency which results from the body's inability to absorb vitamin B12 from the foods eaten.
  • Imerslund's Syndrome: A rare inherited disorder characterized by vitamin B12 deficiency which results from the body's inability to absorb vitamin B12 from the foods eaten.
  • Imerslund-Najman-Grasbeck Anemia: A rare inherited disorder characterized by vitamin B12 deficiency which results from the body's inability to absorb vitamin B12 from the foods eaten.
  • Imerslund-Najman-Grasbeck Disease: A rare inherited disorder characterized by vitamin B12 deficiency which results from the body's inability to absorb vitamin B12 from the foods eaten.
  • Imerslund-Najman-Grasbeck Syndrome: A rare inherited disorder characterized by vitamin B12 deficiency which results from the body's inability to absorb vitamin B12 from the foods eaten.
  • Intrauterine infections: Infection of the fetus while still inside the womb. The type and severity of symptoms is determined by the type of infection and at what stage of pregnancy it occurs. Some cases are mild enough to be asymptomatic and others are severe enough to cause a miscarriage.
  • Juvenile Megaloblastic Anemia: A rare inherited disorder characterized by vitamin B12 deficiency which results from the body's inability to absorb vitamin B12 from the foods eaten.
  • Leukomalacia: Softening or destruction of the white matter of the brain. Brain tissue that surrounds fluid-filled parts of the brain (ventricles) is destroyed. It tends to occur mainly in premature or newborn babies who have been deprived of oxygen or have poor blood flow to parts of the brain. Intrauterine infections and premature membrane rupture tend to predispose infants to this condition. This type of brain destruction can cause cerebral palsy. Severity of symptoms varies according to the degree of injury to the brain.
  • Megalencephaly -- cutis marmorata telangiectatica congenita: A very rare syndrome characterized mainly by an enlarged brain, neurological abnormalities and a blood vessel abnormality that gives the skin a marbled appearance.
  • Megaloblasti Anemia, 1: A rare inherited disorder characterized by vitamin B12 deficiency which results from the body's inability to absorb vitamin B12 from the foods eaten.
  • Megaloblastic Anemia, Familial: A rare inherited disorder characterized by vitamin B12 deficiency which results from the body's inability to absorb vitamin B12 from the foods eaten.
  • Megaloblastic anemia: Megaloblastic anemia, also called pernicious anemia, is a condition in which there is a low number of red blood cells most often caused by a lack of vitamin B12.
  • Mental problems: Symptoms affecting judgement, thought or intelligence.
  • Mitochondrial encephalomyopathy -- aminoacidopathy: A very rare syndrome characterized mainly by muscle and brain disease and an amino acid disorder.
  • Nerve symptoms: Symptoms affecting the nerves
  • Neurological symptoms: Any symptoms that are caused by neurological conditions
  • Neurosyphilis -- general paresis: A complication of untreated syphilis where the infection invades the brain cells and causes a range of neurological symptoms. The condition is progressive and life-threatening.
  • Non-diarrheal (D-) HUS syndrome: A rare condition characterized by hemolytic anemia, thrombocytopenia and kidney failure that is not associated with diarrhea which means that it is not a result of bacterial gastroenteritis. This form of hemolytic uremic syndrome may be caused by kidney transplants, certain drugs (cyclosporine, tacrolimus, cytotoxic drugs), pregnancy, malignancy, HIV, non-diarrheal bacterial infections, immunological conditions or it may be inherited or in some cases there is no obvious cause (idiopathic).
  • Pernicious Anemia, Juvenile type: A rare inherited disorder characterized by vitamin B12 deficiency which results from the body's inability to absorb vitamin B12 from the foods eaten.
  • Peroxisomal defects: A group of metabolic disorders caused by genetic anomalies resulting in dysfunctional peroxisomes. Peroxisomes are found in cells in the body and are involved in functions such as metabolizing certain fatty acids and producing bile acid. Examples of condition involving peroxisomal defects includes Zellweger syndrome and adrenoleukodystrophy. The range and severity of symptoms vary greatly depending on the particular condition involved.
  • Personality symptoms: Symptoms or changes to the personality.
  • Primary lipodystrophies: A group of rare diseases which involve loss of body fat. The body fat loss may be localized to certain parts of the body or may be generalized depending on the particular subtype.
  • Pyruvate carboxylase deficiency, Group B: A rare inherited disorder characterized by a deficiency of pyruvate carboxylase which leads to accumulation of lactic acid and other compounds which can have a toxic effect on the nervous system and body organs. Type B has severe, life-threatening symptoms that can be noticed soon after birth.
  • Retinopathy -- aplastic anemia -- neurological abnormalities: A very rare syndrome characterized by retinal disease, aplastic anemia and neurological problems.
  • Skeletal dysplasia -- mental retardation: A rare recessively inherited disorder characterized mainly by mental retardation, a small head, arthrogryposis (joint contractures), cleft palate and various other abnormalities.
  • Syphilis: A sexually transmitted disease caused by a bacteria (Treponema pallidum). The condition is often asymptomatic in the early stages but one or more sores may be present in the early stages. Untreated syphilis usually results in remission of visible symptoms but further severe damage may occur to internal organs and other body tissues which can result in death.
  • Van Bogaert disease: A rare inherited condition where cholesterol is deposited in the brain and other parts of the body. The disease is classified as a lipid storage disorder due to the abnormal deposition of cholesterol and cholestanol in various parts of the body - especially the brain, lungs and Achilles tendon. The condition is possibly highly underdiagnosed.
  • Van Bogaert's disease: A rare inherited condition where cholesterol is deposited in the brain and other parts of the body. The disease is classified as a lipid storage disorder due to the abnormal deposition of cholesterol and cholestanol in various parts of the body - especially the brain, lungs and Achilles tendon. The condition is possibly highly underdiagnosed.
  • Van Bogaert-Scherer-Epstein Disease: A rare inherited condition where cholesterol is deposited in the brain and other parts of the body. The disease is classified as a lipid storage disorder due to the abnormal deposition of cholesterol and cholestanol in various parts of the body - especially the brain, lungs and Achilles tendon. The condition is possibly highly underdiagnosed.
  • Xanthomatosis cerebrotendinous: A rare inherited condition where cholesterol is deposited in the brain and other parts of the body. The disease is classified as a lipid storage disorder due to the abnormal deposition of cholesterol and cholestanol in various parts of the body - especially the brain, lungs and Achilles tendon. The condition is possibly highly underdiagnosed.

Conditions listing medical symptoms: Neurological problems:

The following list of conditions have 'Neurological problems' or similar listed as a symptom in our database. This computer-generated list may be inaccurate or incomplete. Always seek prompt professional medical advice about the cause of any symptom.

Select from the following alphabetical view of conditions which include a symptom of Neurological problems or choose View All.

View All A B C F G H I J L M N P R S V X

Conditions listing medical complications: Neurological problems:

The following list of medical conditions have 'Neurological problems' or similar listed as a medical complication in our database.

 

By using this site you agree to our Terms of Use. Information provided on this site is for informational purposes only; it is not intended as a substitute for advice from your own medical team. The information on this site is not to be used for diagnosing or treating any health concerns you may have - please contact your physician or health care professional for all your medical needs. Please see our Terms of Use.

Home | Symptoms | Diseases | Diagnosis | Videos | Tools | Forum | About Us | Terms of Use | Privacy Policy | Site Map | Advertise