chromosome 15q24 deletion syndrome
15q24 microdeletion syndrome is a rare chromosomal anomaly characterized cytogenetically by a 1.7-6.1 Mb deletion in chromosome 15q24 and clinically by pre- and post-natal growth retardation, intellectual disability, distinct facial features, and genital, skeletal, and digital anomalies.
Also known as: 15q24 microdeletion syndrome, 15q24 recurrent microdeletion syndrome, Del(15)(q24), chromosome 15q24 deletion syndrome, monosomy 15q24, WITKOS.
Category: General
Symptoms associated with chromosome 15q24 deletion syndrome
The following symptoms have been associated with chromosome 15q24 deletion syndrome in medical literature. Not everyone experiences the same symptoms.
Anxiety
Intense feelings of nervousness, tension, or panic often arise in response to interpersonal stresses. There is...
Constipation
Infrequent or difficult evacuation of feces....
Deeply set eye
An eye that is more deeply recessed into the plane of the face than is typical....
Fatigue
A subjective feeling of tiredness characterized by a lack of energy and motivation....
Gastroesophageal reflux
A condition in which the stomach contents leak backwards from the stomach into the esophagus through the lower...
Hearing impairment
A decreased magnitude of the sensory perception of sound....
Intracranial hemorrhage
Hemorrhage occurring within the skull....
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....
Tests used to investigate chromosome 15q24 deletion syndrome
Healthcare providers may order these tests when evaluating chromosome 15q24 deletion 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 chromosome 15q24 deletion syndrome, which is why a clinical evaluation is important.
Autosomal dominant progressive external ophthalmoplegia
Autosomal dominant progressive external ophthalmoplegia is a medical condition that may be associated with var...
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...
Guillouet-Gordon syndrome
Guillouet-Gordon syndrome is a medical condition that may be associated with various symptoms and signs....
ReNU syndrome
ReNU syndrome is a medical condition that may be associated with various symptoms and signs....
developmental delay, impaired speech, and behavioral abnormalities
developmental delay, impaired speech, and behavioral abnormalities is a medical condition that may be associat...
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 chromosome 15q24 deletion syndrome?
chromosome 15q24 deletion syndrome is a health condition described in medical literature. 15q24 microdeletion syndrome is a rare chromosomal anomaly characterized cytogenetically by a 1.7-6.1 Mb deletion in chromosome 15q24 and clinically by pre- and post-natal growth retardation, intellectual disability, distinct facial features, and genital, skeletal, and digital anomalies.
What are the symptoms of chromosome 15q24 deletion syndrome?
chromosome 15q24 deletion syndrome is associated with 9 symptoms in the medical literature we index, including Anxiety, Constipation, Deeply set eye, Fatigue, Gastroesophageal reflux, Hearing impairment. Symptoms vary widely between individuals.
How is chromosome 15q24 deletion syndrome diagnosed or investigated?
A healthcare provider may use a combination of medical history, physical examination, and tests. Common tests associated with chromosome 15q24 deletion 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 chromosome 15q24 deletion syndrome, please discuss your symptoms with a qualified healthcare provider.