cerebral arteriopathy, autosomal recessive, with subcortical infarcts and leukoencephalopathy 1
cerebral arteriopathy, autosomal recessive, with subcortical infarcts and leukoencephalopathy 1 is a medical condition that may be associated with various symptoms and signs.
Category: General
Symptoms associated with cerebral arteriopathy, autosomal recessive, with subcortical infarcts and leukoencephalopathy 1
The following symptoms have been associated with cerebral arteriopathy, autosomal recessive, with subcortical infarcts and leukoencephalopathy 1 in medical literature. Not everyone experiences the same symptoms.
Bilateral tonic-clonic seizure
A bilateral tonic-clonic seizure is a seizure defined by a tonic (bilateral increased tone, lasting seconds to...
Dysphagia
Difficulty in swallowing....
Facial diplegia
Facial diplegia refers to bilateral facial palsy (bilateral facial palsy is much rarer than unilateral facial ...
Failure to thrive
Failure to thrive (FTT) refers to a child whose physical growth is substantially below the norm....
Fatigue
A subjective feeling of tiredness characterized by a lack of energy and motivation....
Fever
Body temperature elevated above the normal range....
Headache
Cephalgia, or pain sensed in various parts of the head, not confined to the area of distribution of any nerve....
Hemiparesis
Loss of strength in the arm, leg, and sometimes face on one side of the body. Hemiplegia refers to a complete ...
Migraine
Migraine is a chronic neurological disorder characterized by episodic attacks of headache and associated sympt...
Nausea and vomiting
Nausea is a commonly encountered symptom that has been defined as an unpleasant painless subjective feeling th...
Poor suck
An inadequate sucking reflex, resulting in the difficult of newborns to be breast-fed....
Prolonged neonatal jaundice
Neonatal jaundice refers to a yellowing of the skin and other tissues of a newborn infant as a result of incre...
Seizure
A seizure is an intermittent abnormality of nervous system physiology characterized by a transient occurrence ...
Sensorineural hearing impairment
A type of hearing impairment in one or both ears related to an abnormal functionality of the cochlear nerve....
Simple febrile seizure
A short generalized seizure, of a duration of <15 min, not recurring within 24 h, occurring during a febrile e...
Status epilepticus
Status epilepticus is a type of prolonged seizure resulting either from the failure of the mechanisms responsi...
Urinary incontinence
Loss of the ability to control the urinary bladder leading to involuntary urination....
Vertigo
An abnormal sensation of spinning while the body is actually stationary....
Tests used to investigate cerebral arteriopathy, autosomal recessive, with subcortical infarcts and leukoencephalopathy 1
Healthcare providers may order these tests when evaluating cerebral arteriopathy, autosomal recessive, with subcortical infarcts and leukoencephalopathy 1. Test selection is a clinical decision made by a qualified professional.
CBC with Differential
Measures red blood cells, white blood cells, and platelets to help evaluate overall health and detect disorder...
Comprehensive Metabolic Panel (CMP)
Measures 14 substances in the blood to assess kidney and liver function, electrolyte balance, and blood sugar ...
Urinalysis
Examines urine content to help detect urinary tract infections, kidney disease, and diabetes....
Conditions with overlapping symptoms
These conditions share symptoms with cerebral arteriopathy, autosomal recessive, with subcortical infarcts and leukoencephalopathy 1, which is why a clinical evaluation is important.
Autosomal dominant progressive external ophthalmoplegia
Autosomal dominant progressive external ophthalmoplegia is a medical condition that may be associated with var...
Behçet disease
Behçet disease is a medical condition that may be associated with various symptoms and signs....
Granulomatosis with polyangiitis
Granulomatosis with polyangiitis is a medical condition that may be associated with various symptoms and signs...
MELAS
MELAS is a medical condition that may be associated with various symptoms and signs....
Morimoto-Ryu-Malicdan neuromuscular syndrome
Morimoto-Ryu-Malicdan neuromuscular syndrome is a medical condition that may be associated with various sympto...
multiple mitochondrial dysfunctions syndrome 9b
A mitochondrial dysfunction syndrome in which the cause of the disease is a mutation in the FDXR gene. It is c...
Frequently Asked Questions
What is cerebral arteriopathy, autosomal recessive, with subcortical infarcts and leukoencephalopathy 1?
cerebral arteriopathy, autosomal recessive, with subcortical infarcts and leukoencephalopathy 1 is a health condition described in medical literature. cerebral arteriopathy, autosomal recessive, with subcortical infarcts and leukoencephalopathy 1 is a medical condition that may be associated with various symptoms and signs.
What are the symptoms of cerebral arteriopathy, autosomal recessive, with subcortical infarcts and leukoencephalopathy 1?
cerebral arteriopathy, autosomal recessive, with subcortical infarcts and leukoencephalopathy 1 is associated with 18 symptoms in the medical literature we index, including Bilateral tonic-clonic seizure, Dysphagia, Facial diplegia, Failure to thrive, Fatigue, Fever. Symptoms vary widely between individuals.
How is cerebral arteriopathy, autosomal recessive, with subcortical infarcts and leukoencephalopathy 1 diagnosed or investigated?
A healthcare provider may use a combination of medical history, physical examination, and tests. Common tests associated with cerebral arteriopathy, autosomal recessive, with subcortical infarcts and leukoencephalopathy 1 include CBC with Differential, Comprehensive Metabolic Panel (CMP), Urinalysis. This information is educational, not a diagnosis.
Is SymptomDatabase.com diagnosing me?
No. SymptomDatabase.com does not provide diagnosis. If you are concerned you may have cerebral arteriopathy, autosomal recessive, with subcortical infarcts and leukoencephalopathy 1, please discuss your symptoms with a qualified healthcare provider.