Angelman syndrome due to paternal uniparental disomy of chromosome 15
Angelman syndrome due to paternal uniparental disomy of chromosome 15 is a medical condition that may be associated with various symptoms and signs.
Category: General
Symptoms associated with Angelman syndrome due to paternal uniparental disomy of chromosome 15
The following symptoms have been associated with Angelman syndrome due to paternal uniparental disomy of chromosome 15 in medical literature. Not everyone experiences the same symptoms.
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...
Dysphagia
Difficulty in swallowing....
Generalised tonic-clonic seizure without focal onset
A bilateral tonic-clonic seizure with generalized onset is a type of bilateral tonic-clonic seizure characteri...
Heat intolerance
The inability to maintain a comfortable body temperature in warm or hot weather....
Poor suck
An inadequate sucking reflex, resulting in the difficult of newborns to be breast-fed....
Seizure
A seizure is an intermittent abnormality of nervous system physiology characterized by a transient occurrence ...
Tests used to investigate Angelman syndrome due to paternal uniparental disomy of chromosome 15
Healthcare providers may order these tests when evaluating Angelman syndrome due to paternal uniparental disomy of chromosome 15. 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 Angelman syndrome due to paternal uniparental disomy of chromosome 15, which is why a clinical evaluation is important.
DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion
DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion is a medical condition that...
Early infantile developmental and epileptic encephalopathy
Early infantile developmental and epileptic encephalopathy is a medical condition that may be associated with ...
Landau-Kleffner syndrome
Landau-Kleffner syndrome is a medical condition that may be associated with various symptoms and signs....
cerebral arteriopathy, autosomal recessive, with subcortical infarcts and leukoencephalopathy 1
cerebral arteriopathy, autosomal recessive, with subcortical infarcts and leukoencephalopathy 1 is a medical c...
neurodevelopmental disorder with growth impairment, quadriparesis, and poor or absent speech
neurodevelopmental disorder with growth impairment, quadriparesis, and poor or absent speech is a medical cond...
neurodevelopmental disorder with hypotonia and speech delay, with or without seizures
neurodevelopmental disorder with hypotonia and speech delay, with or without seizures is a medical condition t...
Frequently Asked Questions
What is Angelman syndrome due to paternal uniparental disomy of chromosome 15?
Angelman syndrome due to paternal uniparental disomy of chromosome 15 is a health condition described in medical literature. Angelman syndrome due to paternal uniparental disomy of chromosome 15 is a medical condition that may be associated with various symptoms and signs.
What are the symptoms of Angelman syndrome due to paternal uniparental disomy of chromosome 15?
Angelman syndrome due to paternal uniparental disomy of chromosome 15 is associated with 7 symptoms in the medical literature we index, including Atypical absence seizure, Bilateral tonic-clonic seizure, Dysphagia, Generalised tonic-clonic seizure without focal onset, Heat intolerance, Poor suck. Symptoms vary widely between individuals.
How is Angelman syndrome due to paternal uniparental disomy of chromosome 15 diagnosed or investigated?
A healthcare provider may use a combination of medical history, physical examination, and tests. Common tests associated with Angelman syndrome due to paternal uniparental disomy of chromosome 15 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 Angelman syndrome due to paternal uniparental disomy of chromosome 15, please discuss your symptoms with a qualified healthcare provider.