Methylcobalamin deficiency type cblE
Methylcobalamin deficiency type cblE is a medical condition that may be associated with various symptoms and signs.
Category: General
Symptoms associated with Methylcobalamin deficiency type cblE
The following symptoms have been associated with Methylcobalamin deficiency type cblE in medical literature. Not everyone experiences the same symptoms.
Drowsiness
Abnormal feeling of sleepiness or difficulty staying awake....
Excessive daytime somnolence
A state of abnormally strong desire for sleep during the daytime....
Failure to thrive
Failure to thrive (FTT) refers to a child whose physical growth is substantially below the norm....
Hearing impairment
A decreased magnitude of the sensory perception of sound....
Hypertension
The presence of chronic increased pressure in the systemic arterial system....
Seizure
A seizure is an intermittent abnormality of nervous system physiology characterized by a transient occurrence ...
Vomiting
Forceful ejection of the contents of the stomach through the mouth by means of a series of involuntary spasmic...
Tests used to investigate Methylcobalamin deficiency type cblE
Healthcare providers may order these tests when evaluating Methylcobalamin deficiency type cblE. 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 Methylcobalamin deficiency type cblE, which is why a clinical evaluation is important.
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Prader-Willi syndrome
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RNU5B-1 related neurodevelopmental disorder with seizures and joint laxity
A neurodevelopmental disorder in which the cause of the disease is a variation in RNU5B-1 gene and is characte...
Smith-Lemli-Opitz syndrome
Smith-Lemli-Opitz syndrome (SLOS) is characterized by multiple congenital anomalies, intellectual deficit, and...
mitochondrial DNA depletion syndrome 6 (hepatocerebral type)
mitochondrial DNA depletion syndrome 6 (hepatocerebral type) is a medical condition that may be associated wit...
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 Methylcobalamin deficiency type cblE?
Methylcobalamin deficiency type cblE is a health condition described in medical literature. Methylcobalamin deficiency type cblE is a medical condition that may be associated with various symptoms and signs.
What are the symptoms of Methylcobalamin deficiency type cblE?
Methylcobalamin deficiency type cblE is associated with 7 symptoms in the medical literature we index, including Drowsiness, Excessive daytime somnolence, Failure to thrive, Hearing impairment, Hypertension, Seizure. Symptoms vary widely between individuals.
How is Methylcobalamin deficiency type cblE diagnosed or investigated?
A healthcare provider may use a combination of medical history, physical examination, and tests. Common tests associated with Methylcobalamin deficiency type cblE 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 Methylcobalamin deficiency type cblE, please discuss your symptoms with a qualified healthcare provider.