Cerebrotendinous xanthomatosis
Related Gene(s)
References
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Cerebrotendinous Xanthomatosis
Cerebrotendinous Xanthomatosis
This treatable disorder has serious eye and neurologic manifestations.
Alternate Names : Type II hyperlipoproteinemia, Hypercholesterolemic xanthomatosis, Low density lipoprotein receptor mutation
Definition ...
xanthomatosis
znm tss noun a condition in which several small masses of yellow fatty substance appear in the skin or ...
xenograft ...
Xanthomatosis cerebrotendinous ... depression
Y
Young Simpson syndrome ... Depression ...
Cerebrotendinous Xanthomatosis
Cerebrovascular Accident (Stroke)
Cerebrovascular Accident, Antiplatelets for - Medication
Cerebrovascular Accident, Aspirin for - Medication
Cerebrovascular Accident, Carotid Endarterectomy for ...
Cerebrotendinous xanthomatosis
Comorbidities and complications of type 2 diabetes mellitus in children and adolescents
Definition and diagnosis of hypertension in children and adolescents
Diseases associated with atherosclerosis in childhood ...
Neuronal ceroid lipofuscinosis (Batten disease) - Cerebrotendineous xanthomatosis - Cholesteryl ester storage disease (Wolman disease)
Fatty acid metabolism ...
Type II hyperlipoproteinemia; Hypercholesterolemic xanthomatosis; Low density lipoprotein receptor mutation
Causes
Familial hypercholesterolemia is a genetic disorder caused by a defect on chromosome 19.
Histamine, IGF Binding Protein 4, Immunolabeling Technics, Infection, Roseolovirus, Kallikrein, hK3, Leriches Syndrome, Mandrill, Monkey, Red, Neonatal Citrullinemias, Neoplasm, Benign Infratentorial, Neurogenic Bladder Disorders, Xanthomatosis, ...
(Also Called 'CACH (Central Hypomyelination)', 'Central Hypomyelination', 'Cerebrotendinous Xanthomatosis')
What is Leukodystrophy?
Other diabetic skin diseases are seen mainly or exclusively in people with diabetes as is the case, for example, with diabetic dermopathy, necrobiosis lipoidica diabeticorum (NLD), diabetic blisters (bullosis diabeticorum), and eruptive xanthomatosis.
Autosomal recessive ataxias include Friedreich's ataxia (the most prevalent), ataxia-telangiectasia, abetalipoproteinemia, ataxia with isolated vitamin E deficiency, and cerebrotendinous xanthomatosis.
Pelizaeus-Merzbacher disease
Canavan disease
Childhood ataxia with central nervous system hypomyelination (CACH, also called vanishing white matter disease)
Alexander disease
Refsum disease
Cerebrotendinous xanthomatosis ...
Fabrys, Gauchers, I Cell [Mucolipidosis I], Lipoid Storage NOS, Niemann-Pick, Pseudo-Hurlers or Mucolipidosis III, Triglyceride Storage, Type I or II, Wolmans or Triglyceride Storage, Type III; Mucolipidosis II; Primary Familial Xanthomatosis ...
Treatment includes changes to diet, regular exercise, avoiding smoking, and the use of cholesterol-lowering drugs. Other names for familial hypercholesterolaemia include familial hyperlipidaemia, hypercholesterolaemic xanthomatosis and low density ...
Cerebrotendinous Xanthomatosis
Cerebrovascular Accident (Stroke)
Cerebrovascular Accident, Carotid Endarterectomy for
cerebrovascular ferrocalcinosis
Ceroid-Lipofuscinosis, Adult form
Cervical biopsy for abnormal cervical cell changes ...
Hypercholesterolemic xanthomatosis
Hypercoagulable states
Hypercortisolism
Hyperemesis gravidarum
Encyclopedia Article
Encyclopedia Article
Hyperimmunization
Hyperimmunoglobulin E syndrome
Hyperkalemia
Hyperkalemic periodic paralysis ...
 See also: Symptom, Deficiency, Cholesterol, Sclerosis, Dystrophy
  
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