Cross syndrome: Difference between revisions
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[[File:Autosomal_recessive_-_en.svg| | {{SI}} | ||
{{Infobox medical condition | |||
| name = Cross syndrome | |||
| image = [[File:Autosomal_recessive_-_en.svg|200px]] | |||
| caption = Cross syndrome is inherited in an [[autosomal recessive]] pattern. | |||
| synonyms = | |||
| pronounce = | |||
| specialty = [[Medical genetics]] | |||
| symptoms = [[Intellectual disability]], [[epilepsy]], [[microcephaly]], [[spasticity]] | |||
| onset = [[Infancy]] | |||
| duration = [[Lifelong]] | |||
| causes = Mutations in the [[ITGB2]] gene | |||
| risks = | |||
| diagnosis = [[Genetic testing]], [[clinical evaluation]] | |||
| differential = [[Cerebral palsy]], [[Rett syndrome]] | |||
| treatment = [[Supportive care]], [[physical therapy]], [[anticonvulsants]] | |||
| medication = [[Anticonvulsants]] | |||
| prognosis = Variable, depends on severity | |||
| frequency = Rare | |||
| deaths = | |||
}} | |||
'''Cross syndrome''' is a rare [[genetic disorder]] characterized by a combination of [[physical]] and [[neurological]] abnormalities. It is named after the physician who first described the condition. The syndrome is typically diagnosed in [[infancy]] or early [[childhood]]. | |||
== Symptoms == | == Symptoms == | ||
Individuals with Cross syndrome may exhibit a variety of symptoms, including: | Individuals with Cross syndrome may exhibit a variety of symptoms, including: | ||
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* [[Seizures]] | * [[Seizures]] | ||
* [[Feeding difficulties]] | * [[Feeding difficulties]] | ||
== Causes == | == Causes == | ||
Cross syndrome is caused by mutations in a specific [[gene]] located on a particular [[chromosome]]. The exact genetic mechanism can vary, but it often involves a [[de novo mutation]], meaning it occurs spontaneously and is not inherited from either parent. | Cross syndrome is caused by mutations in a specific [[gene]] located on a particular [[chromosome]]. The exact genetic mechanism can vary, but it often involves a [[de novo mutation]], meaning it occurs spontaneously and is not inherited from either parent. | ||
== Diagnosis == | == Diagnosis == | ||
Diagnosis of Cross syndrome typically involves a combination of: | Diagnosis of Cross syndrome typically involves a combination of: | ||
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* [[Imaging studies]] such as [[MRI]] or [[CT scan]] | * [[Imaging studies]] such as [[MRI]] or [[CT scan]] | ||
* [[Electroencephalogram]] (EEG) to assess for [[seizure]] activity | * [[Electroencephalogram]] (EEG) to assess for [[seizure]] activity | ||
== Treatment == | == Treatment == | ||
There is no cure for Cross syndrome, and treatment is primarily supportive and symptomatic. Management strategies may include: | There is no cure for Cross syndrome, and treatment is primarily supportive and symptomatic. Management strategies may include: | ||
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* [[Medications]] to control seizures and other symptoms | * [[Medications]] to control seizures and other symptoms | ||
* [[Surgical interventions]] for congenital heart defects or other structural abnormalities | * [[Surgical interventions]] for congenital heart defects or other structural abnormalities | ||
== Prognosis == | == Prognosis == | ||
The prognosis for individuals with Cross syndrome varies widely depending on the severity of symptoms and the presence of associated conditions. Early intervention and supportive care can significantly improve the quality of life for affected individuals. | The prognosis for individuals with Cross syndrome varies widely depending on the severity of symptoms and the presence of associated conditions. Early intervention and supportive care can significantly improve the quality of life for affected individuals. | ||
== See also == | == See also == | ||
* [[Genetic disorder]] | * [[Genetic disorder]] | ||
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* [[Congenital heart defect]] | * [[Congenital heart defect]] | ||
* [[Seizure]] | * [[Seizure]] | ||
== References == | == References == | ||
{{Reflist}} | {{Reflist}} | ||
== External links == | == External links == | ||
{{No external links}} | {{No external links}} | ||
[[Category:Genetic disorders]] | [[Category:Genetic disorders]] | ||
[[Category:Neurological disorders]] | [[Category:Neurological disorders]] | ||
[[Category:Rare diseases]] | [[Category:Rare diseases]] | ||
[[Category:Pediatrics]] | [[Category:Pediatrics]] | ||
{{Genetic-disorder-stub}} | {{Genetic-disorder-stub}} | ||
Latest revision as of 13:37, 5 April 2025

Editor-In-Chief: Prab R Tumpati, MD
Obesity, Sleep & Internal medicine
Founder, WikiMD Wellnesspedia &
W8MD medical weight loss NYC and sleep center NYC
| Cross syndrome | |
|---|---|
| Synonyms | |
| Pronounce | |
| Specialty | Medical genetics |
| Symptoms | Intellectual disability, epilepsy, microcephaly, spasticity |
| Complications | N/A |
| Onset | Infancy |
| Duration | Lifelong |
| Types | N/A |
| Causes | Mutations in the ITGB2 gene |
| Risks | |
| Diagnosis | Genetic testing, clinical evaluation |
| Differential diagnosis | Cerebral palsy, Rett syndrome |
| Prevention | N/A |
| Treatment | Supportive care, physical therapy, anticonvulsants |
| Medication | Anticonvulsants |
| Prognosis | Variable, depends on severity |
| Frequency | Rare |
| Deaths | |
Cross syndrome is a rare genetic disorder characterized by a combination of physical and neurological abnormalities. It is named after the physician who first described the condition. The syndrome is typically diagnosed in infancy or early childhood.
Symptoms[edit]
Individuals with Cross syndrome may exhibit a variety of symptoms, including:
- Developmental delay
- Intellectual disability
- Hypotonia (reduced muscle tone)
- Distinctive facial features such as a broad forehead, wide-set eyes, and a small chin
- Congenital heart defects
- Seizures
- Feeding difficulties
Causes[edit]
Cross syndrome is caused by mutations in a specific gene located on a particular chromosome. The exact genetic mechanism can vary, but it often involves a de novo mutation, meaning it occurs spontaneously and is not inherited from either parent.
Diagnosis[edit]
Diagnosis of Cross syndrome typically involves a combination of:
- Clinical evaluation
- Genetic testing
- Imaging studies such as MRI or CT scan
- Electroencephalogram (EEG) to assess for seizure activity
Treatment[edit]
There is no cure for Cross syndrome, and treatment is primarily supportive and symptomatic. Management strategies may include:
- Physical therapy to improve muscle tone and coordination
- Occupational therapy to assist with daily living skills
- Speech therapy to address communication difficulties
- Medications to control seizures and other symptoms
- Surgical interventions for congenital heart defects or other structural abnormalities
Prognosis[edit]
The prognosis for individuals with Cross syndrome varies widely depending on the severity of symptoms and the presence of associated conditions. Early intervention and supportive care can significantly improve the quality of life for affected individuals.
See also[edit]
References[edit]
<references group="" responsive="1"></references>
External links[edit]
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