developmental and epileptic encephalopathy, 31A
Any developmental and epileptic encephalopathy in which the cause of the disease is a heterozygous mutation in the DNM1 gene.
Also known as: DEE31, DNM1-encephalopathy and neurodevelopmental disorder, DNM1-related epilepsy and neurodevelopmental disorder, EIEE31, developmental and epileptic encephalopathy 31, early infantile epileptic encephalopathy caused by mutation in DNM1, epileptic encephalopathy, early infantile, 31, epileptic encephalopathy, early infantile, type 31, DEE31A, DNM1 early infantile epileptic encephalopathy.
Category: General
Symptoms associated with developmental and epileptic encephalopathy, 31A
The following symptoms have been associated with developmental and epileptic encephalopathy, 31A in medical literature. Not everyone experiences the same symptoms.
Atonic seizure
Atonic seizure is a type of motor seizure characterized by a sudden loss or diminution of muscle tone without ...
Atypical absence seizure
An atypical absence seizure is a type of generalized non-motor (absence) seizure characterized by interruption...
Bilateral tonic-clonic seizure
A bilateral tonic-clonic seizure is a seizure defined by a tonic (bilateral increased tone, lasting seconds to...
Epileptic spasm
A sudden flexion, extension, or mixed extension-flexion of predominantly proximal and truncal muscles that is ...
Focal impaired awareness seizure
Focal impaired awareness seizure (or focal seizure with impaired or lost awareness) is a type of focal-onset s...
Myoclonic seizure
A myoclonic seizure is a type of motor seizure characterized by sudden, brief (<100 ms) involuntary single or ...
Tonic seizure
A tonic seizure is a type of motor seizure characterized by unilateral or bilateral limb stiffening or elevati...
Tests used to investigate developmental and epileptic encephalopathy, 31A
Healthcare providers may order these tests when evaluating developmental and epileptic encephalopathy, 31A. 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 developmental and epileptic encephalopathy, 31A, 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...
developmental and epileptic encephalopathy 103
developmental and epileptic encephalopathy 103 is a medical condition that may be associated with various symp...
developmental and epileptic encephalopathy 119
A developmental and epileptic encephalopathy caused by the variants in the RNU2-2 gene, in which most reported...
developmental and epileptic encephalopathy 120
developmental and epileptic encephalopathy 120 is a medical condition that may be associated with various symp...
developmental and epileptic encephalopathy, 74
developmental and epileptic encephalopathy, 74 is a medical condition that may be associated with various symp...
lissencephaly 10
lissencephaly 10 is a medical condition that may be associated with various symptoms and signs....
Frequently Asked Questions
What is developmental and epileptic encephalopathy, 31A?
developmental and epileptic encephalopathy, 31A is a health condition described in medical literature. Any developmental and epileptic encephalopathy in which the cause of the disease is a heterozygous mutation in the DNM1 gene.
What are the symptoms of developmental and epileptic encephalopathy, 31A?
developmental and epileptic encephalopathy, 31A is associated with 7 symptoms in the medical literature we index, including Atonic seizure, Atypical absence seizure, Bilateral tonic-clonic seizure, Epileptic spasm, Focal impaired awareness seizure, Myoclonic seizure. Symptoms vary widely between individuals.
How is developmental and epileptic encephalopathy, 31A diagnosed or investigated?
A healthcare provider may use a combination of medical history, physical examination, and tests. Common tests associated with developmental and epileptic encephalopathy, 31A 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 developmental and epileptic encephalopathy, 31A, please discuss your symptoms with a qualified healthcare provider.