Heart-hand syndromes: Difference between revisions
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{{Infobox medical condition | |||
| name = Heart-hand syndromes | |||
| image = [[200px]] | |||
| caption = Heart-hand syndromes are often inherited in an [[autosomal dominant]] pattern. | |||
| synonyms = Cardiovascular-limb syndromes | |||
| field = [[Medical genetics]] | |||
| symptoms = [[Congenital heart defect]], [[limb anomalies]] | |||
| onset = [[Congenital]] | |||
| duration = Lifelong | |||
| causes = [[Genetic mutation]] | |||
| risks = Family history of the condition | |||
| diagnosis = [[Genetic testing]], [[echocardiogram]], [[X-ray]] | |||
| differential = [[Holt–Oram syndrome]], [[Ellis–van Creveld syndrome]], [[Noonan syndrome]] | |||
| treatment = [[Surgical intervention]], [[cardiac care]], [[physical therapy]] | |||
| prognosis = Varies depending on severity | |||
| frequency = Rare | |||
}} | |||
'''Heart-hand syndromes''' are a group of [[genetic disorder|genetic disorders]] that primarily affect the [[heart]] and the [[hand|hands]]. These syndromes are characterized by [[congenital heart disease]] and hand abnormalities. | '''Heart-hand syndromes''' are a group of [[genetic disorder|genetic disorders]] that primarily affect the [[heart]] and the [[hand|hands]]. These syndromes are characterized by [[congenital heart disease]] and hand abnormalities. | ||
== Introduction == | |||
== | |||
Heart-hand syndromes are rare genetic disorders. They are characterized by heart disease and hand abnormalities. The heart disease can be congenital, meaning it is present at birth, or it can develop later in life. The hand abnormalities can include deformities of the fingers and hands, such as [[syndactyly]] (fused fingers) or [[brachydactyly]] (short fingers). | Heart-hand syndromes are rare genetic disorders. They are characterized by heart disease and hand abnormalities. The heart disease can be congenital, meaning it is present at birth, or it can develop later in life. The hand abnormalities can include deformities of the fingers and hands, such as [[syndactyly]] (fused fingers) or [[brachydactyly]] (short fingers). | ||
== Types of Heart-Hand Syndromes == | == Types of Heart-Hand Syndromes == | ||
There are several types of heart-hand syndromes, including: | There are several types of heart-hand syndromes, including: | ||
* '''[[Holt-Oram syndrome]]''' - This syndrome is characterized by abnormalities of the upper limbs and heart defects. | * '''[[Holt-Oram syndrome]]''' - This syndrome is characterized by abnormalities of the upper limbs and heart defects. | ||
* '''[[Tabatznik syndrome]]''' - This syndrome is characterized by short stature, heart defects, and hand abnormalities. | * '''[[Tabatznik syndrome]]''' - This syndrome is characterized by short stature, heart defects, and hand abnormalities. | ||
* '''[[Heart-hand syndrome, Slovenian type]]''' - This syndrome is characterized by heart defects, hand abnormalities, and intellectual disability. | * '''[[Heart-hand syndrome, Slovenian type]]''' - This syndrome is characterized by heart defects, hand abnormalities, and intellectual disability. | ||
== Causes == | == Causes == | ||
Heart-hand syndromes are caused by mutations in various [[gene|genes]]. The specific genes involved can vary depending on the type of heart-hand syndrome. These mutations are usually inherited in an [[autosomal dominant]] manner, which means one copy of the altered gene in each cell is sufficient to cause the disorder. | Heart-hand syndromes are caused by mutations in various [[gene|genes]]. The specific genes involved can vary depending on the type of heart-hand syndrome. These mutations are usually inherited in an [[autosomal dominant]] manner, which means one copy of the altered gene in each cell is sufficient to cause the disorder. | ||
== Diagnosis == | == Diagnosis == | ||
Diagnosis of heart-hand syndromes is based on the presence of characteristic signs and symptoms. Genetic testing can confirm the diagnosis. | Diagnosis of heart-hand syndromes is based on the presence of characteristic signs and symptoms. Genetic testing can confirm the diagnosis. | ||
== Treatment == | == Treatment == | ||
Treatment for heart-hand syndromes is focused on managing the symptoms. This can include surgery to correct heart defects or hand abnormalities, as well as therapies to manage other symptoms. | Treatment for heart-hand syndromes is focused on managing the symptoms. This can include surgery to correct heart defects or hand abnormalities, as well as therapies to manage other symptoms. | ||
== See also == | == See also == | ||
* [[Congenital heart disease]] | * [[Congenital heart disease]] | ||
* [[Genetic disorder]] | * [[Genetic disorder]] | ||
| Line 32: | Line 37: | ||
* [[Tabatznik syndrome]] | * [[Tabatznik syndrome]] | ||
* [[Heart-hand syndrome, Slovenian type]] | * [[Heart-hand syndrome, Slovenian type]] | ||
== References == | == References == | ||
<references /> | <references /> | ||
{{stub}} | {{stub}} | ||
[[Category:Genetic disorders]] | [[Category:Genetic disorders]] | ||
[[Category:Congenital disorders]] | [[Category:Congenital disorders]] | ||
[[Category:Rare diseases]] | [[Category:Rare diseases]] | ||
[[Category:Syndromes]] | [[Category:Syndromes]] | ||
Latest revision as of 20:26, 6 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
| Heart-hand syndromes | |
|---|---|
| 200px | |
| Synonyms | Cardiovascular-limb syndromes |
| Pronounce | N/A |
| Specialty | N/A |
| Symptoms | Congenital heart defect, limb anomalies |
| Complications | N/A |
| Onset | Congenital |
| Duration | Lifelong |
| Types | N/A |
| Causes | Genetic mutation |
| Risks | Family history of the condition |
| Diagnosis | Genetic testing, echocardiogram, X-ray |
| Differential diagnosis | Holt–Oram syndrome, Ellis–van Creveld syndrome, Noonan syndrome |
| Prevention | N/A |
| Treatment | Surgical intervention, cardiac care, physical therapy |
| Medication | N/A |
| Prognosis | Varies depending on severity |
| Frequency | Rare |
| Deaths | N/A |
Heart-hand syndromes are a group of genetic disorders that primarily affect the heart and the hands. These syndromes are characterized by congenital heart disease and hand abnormalities.
Introduction[edit]
Heart-hand syndromes are rare genetic disorders. They are characterized by heart disease and hand abnormalities. The heart disease can be congenital, meaning it is present at birth, or it can develop later in life. The hand abnormalities can include deformities of the fingers and hands, such as syndactyly (fused fingers) or brachydactyly (short fingers).
Types of Heart-Hand Syndromes[edit]
There are several types of heart-hand syndromes, including:
- Holt-Oram syndrome - This syndrome is characterized by abnormalities of the upper limbs and heart defects.
- Tabatznik syndrome - This syndrome is characterized by short stature, heart defects, and hand abnormalities.
- Heart-hand syndrome, Slovenian type - This syndrome is characterized by heart defects, hand abnormalities, and intellectual disability.
Causes[edit]
Heart-hand syndromes are caused by mutations in various genes. The specific genes involved can vary depending on the type of heart-hand syndrome. These mutations are usually inherited in an autosomal dominant manner, which means one copy of the altered gene in each cell is sufficient to cause the disorder.
Diagnosis[edit]
Diagnosis of heart-hand syndromes is based on the presence of characteristic signs and symptoms. Genetic testing can confirm the diagnosis.
Treatment[edit]
Treatment for heart-hand syndromes is focused on managing the symptoms. This can include surgery to correct heart defects or hand abnormalities, as well as therapies to manage other symptoms.
See also[edit]
- Congenital heart disease
- Genetic disorder
- Holt-Oram syndrome
- Tabatznik syndrome
- Heart-hand syndrome, Slovenian type
References[edit]
<references />


