CODAS syndrome
Codas syndrome is a multiple congenital anomalies syndrome characterized by Cerebral, Ocular, Dental, Auricular and Skeletal anomalies.
Also known as: CODAS syndrome, cerebrooculodentoauriculoskeletal syndrome, cerebral, ocular, dental, auricular, and skeletal syndrome, cerebro-oculo-dento-auriculo-skeletal syndrome.
Category: General
Symptoms associated with CODAS syndrome
The following symptoms have been associated with CODAS syndrome in medical literature. Not everyone experiences the same symptoms.
Conductive hearing impairment
An abnormality of vibrational conductance of sound to the inner ear leading to impairment of sensory perceptio...
Dysphagia
Difficulty in swallowing....
Gastroesophageal reflux
A condition in which the stomach contents leak backwards from the stomach into the esophagus through the lower...
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 ...
Sensorineural hearing impairment
A type of hearing impairment in one or both ears related to an abnormal functionality of the cochlear nerve....
Vocal cord paresis
Decreased strength of the vocal folds....
Tests used to investigate CODAS syndrome
Healthcare providers may order these tests when evaluating CODAS syndrome. 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 CODAS syndrome, which is why a clinical evaluation is important.
1p36 deletion syndrome
1p36 deletion syndrome is a medical condition that may be associated with various symptoms and signs....
Guillouet-Gordon syndrome
Guillouet-Gordon syndrome is a medical condition that may be associated with various symptoms and signs....
Mucopolysaccharidosis type 3
Mucopolysaccharidosis type 3 is a medical condition that may be associated with various symptoms and signs....
WAC-related facial dysmorphism-developmental delay-behavioral abnormalities syndrome
WAC-related facial dysmorphism-developmental delay-behavioral abnormalities syndrome is a medical condition th...
chromosome 1p36 deletion syndrome
A chromosomal anomaly characterized by distinctive facial dysmorphic features, hypotonia, developmental delay,...
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 CODAS syndrome?
CODAS syndrome is a health condition described in medical literature. Codas syndrome is a multiple congenital anomalies syndrome characterized by Cerebral, Ocular, Dental, Auricular and Skeletal anomalies.
What are the symptoms of CODAS syndrome?
CODAS syndrome is associated with 7 symptoms in the medical literature we index, including Conductive hearing impairment, Dysphagia, Gastroesophageal reflux, Generalized tonic seizure, Seizure, Sensorineural hearing impairment. Symptoms vary widely between individuals.
How is CODAS syndrome diagnosed or investigated?
A healthcare provider may use a combination of medical history, physical examination, and tests. Common tests associated with CODAS syndrome 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 CODAS syndrome, please discuss your symptoms with a qualified healthcare provider.