congenital disorder of glycosylation, type IIcc
congenital disorder of glycosylation, type IIcc is a medical condition that may be associated with various symptoms and signs.
Category: General
Symptoms associated with congenital disorder of glycosylation, type IIcc
The following symptoms have been associated with congenital disorder of glycosylation, type IIcc in medical literature. Not everyone experiences the same symptoms.
Anxiety
Intense feelings of nervousness, tension, or panic often arise in response to interpersonal stresses. There is...
Bilateral tonic-clonic seizure
A bilateral tonic-clonic seizure is a seizure defined by a tonic (bilateral increased tone, lasting seconds to...
Clonic seizure
A clonic seizure is a type of motor seizure characterized by sustained rhythmic jerking, that is regularly rep...
Febrile convulsion
A febrile seizure is any type of seizure (most often a generalized tonic-clonic seizure) occurring with fever ...
Focal impaired awareness seizure
Focal impaired awareness seizure (or focal seizure with impaired or lost awareness) is a type of focal-onset s...
Focal-onset seizure
A focal-onset seizure is a type of seizure originating within networks limited to one hemisphere. They may be ...
Generalised tonic-clonic seizure without focal onset
A bilateral tonic-clonic seizure with generalized onset is a type of bilateral tonic-clonic seizure characteri...
Hearing impairment
A decreased magnitude of the sensory perception of sound....
Myoclonic absence seizure
Myoclonic absence seizure is a type of generalized non-motor (absence) seizure characterized by an interruptio...
Seizure
A seizure is an intermittent abnormality of nervous system physiology characterized by a transient occurrence ...
Status epilepticus
Status epilepticus is a type of prolonged seizure resulting either from the failure of the mechanisms responsi...
Tonic seizure
A tonic seizure is a type of motor seizure characterized by unilateral or bilateral limb stiffening or elevati...
Tremor
An unintentional, oscillating to-and-fro muscle movement about a joint axis....
Tests used to investigate congenital disorder of glycosylation, type IIcc
Healthcare providers may order these tests when evaluating congenital disorder of glycosylation, type IIcc. 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 congenital disorder of glycosylation, type IIcc, which is why a clinical evaluation is important.
Developmental and epileptic encephalopathy 122
Developmental and epileptic encephalopathy 122 is a medical condition that may be associated with various symp...
Houge-Janssens syndrome 4
Houge-Janssens syndrome 4 is a medical condition that may be associated with various symptoms and signs....
Stolerman neurodevelopmental syndrome
Stolerman neurodevelopmental syndrome is a medical condition that may be associated with various symptoms and ...
developmental and epileptic encephalopathy 119
A developmental and epileptic encephalopathy caused by the variants in the RNU2-2 gene, in which most reported...
intellectual disability, autosomal dominant 42
Any autosomal dominant intellectual disability in which the cause of the disease is a heterozygous mutation in...
neurodevelopmental disorder with speech delay, movement abnormalities, and seizures
A neurodevelopmental disorder caused by a variation in the UNC13A gene, characterized by variable degrees of d...
Frequently Asked Questions
What is congenital disorder of glycosylation, type IIcc?
congenital disorder of glycosylation, type IIcc is a health condition described in medical literature. congenital disorder of glycosylation, type IIcc is a medical condition that may be associated with various symptoms and signs.
What are the symptoms of congenital disorder of glycosylation, type IIcc?
congenital disorder of glycosylation, type IIcc is associated with 13 symptoms in the medical literature we index, including Anxiety, Bilateral tonic-clonic seizure, Clonic seizure, Febrile convulsion, Focal impaired awareness seizure, Focal-onset seizure. Symptoms vary widely between individuals.
How is congenital disorder of glycosylation, type IIcc diagnosed or investigated?
A healthcare provider may use a combination of medical history, physical examination, and tests. Common tests associated with congenital disorder of glycosylation, type IIcc 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 congenital disorder of glycosylation, type IIcc, please discuss your symptoms with a qualified healthcare provider.