DPM1-CDG
DPM1-CDG is a medical condition that may be associated with various symptoms and signs.
Category: General
Symptoms associated with DPM1-CDG
The following symptoms have been associated with DPM1-CDG 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 ...
Diarrhea
Abnormally increased frequency (usually defined as three or more) loose or watery bowel movements a day....
Early onset absence seizures
Typical absence seizures starting before the age of 4 years....
Failure to thrive
Failure to thrive (FTT) refers to a child whose physical growth is substantially below the norm....
Generalized myoclonic seizure
A generalized myoclonic seizure is a type of generalized motor seizure characterized by bilateral, sudden, bri...
Generalized tonic seizure
A generalized tonic seizure is a type of generalized motor seizure characterized by bilateral limb stiffening ...
Seizure
A seizure is an intermittent abnormality of nervous system physiology characterized by a transient occurrence ...
Tests used to investigate DPM1-CDG
Healthcare providers may order these tests when evaluating DPM1-CDG. 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 DPM1-CDG, which is why a clinical evaluation is important.
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Lissencephaly due to LIS1 mutation
Lissencephaly due to LIS1 mutation is a medical condition that may be associated with various symptoms and sig...
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...
mitochondrial DNA depletion syndrome 6 (hepatocerebral type)
mitochondrial DNA depletion syndrome 6 (hepatocerebral type) is a medical condition that may be associated wit...
Frequently Asked Questions
What is DPM1-CDG?
DPM1-CDG is a health condition described in medical literature. DPM1-CDG is a medical condition that may be associated with various symptoms and signs.
What are the symptoms of DPM1-CDG?
DPM1-CDG is associated with 7 symptoms in the medical literature we index, including Atonic seizure, Diarrhea, Early onset absence seizures, Failure to thrive, Generalized myoclonic seizure, Generalized tonic seizure. Symptoms vary widely between individuals.
How is DPM1-CDG diagnosed or investigated?
A healthcare provider may use a combination of medical history, physical examination, and tests. Common tests associated with DPM1-CDG 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 DPM1-CDG, please discuss your symptoms with a qualified healthcare provider.