Overgrowth syndrome: Difference between revisions

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{{Infobox medical condition
| name            = Overgrowth syndrome
| synonyms        =
| field          = [[Medical genetics]]
| symptoms        = [[Excessive growth]], [[developmental delay]], [[intellectual disability]], [[macrocephaly]], [[organomegaly]]
| complications  = [[Tumor]] development, [[cardiovascular abnormalities]], [[orthopedic issues]]
| onset          = [[Prenatal]] or [[early childhood]]
| duration        = [[Lifelong]]
| causes          = [[Genetic mutation]]
| risks          = [[Family history]], [[genetic predisposition]]
| diagnosis      = [[Clinical evaluation]], [[genetic testing]]
| differential    = [[Gigantism]], [[Beckwith-Wiedemann syndrome]], [[Sotos syndrome]]
| prevention      = None
| treatment      = [[Symptomatic treatment]], [[surgical intervention]]
| medication      =
| prognosis      = Variable, depending on specific syndrome and complications
| frequency      = Rare
}}
'''Overgrowth syndrome''' is a term used to describe a group of [[genetic disorders]] characterized by an increased growth rate, often resulting in an abnormally large size for a person's age or stage of development. These syndromes can affect multiple parts of the body, including the bones, muscles, skin, and internal organs.  
'''Overgrowth syndrome''' is a term used to describe a group of [[genetic disorders]] characterized by an increased growth rate, often resulting in an abnormally large size for a person's age or stage of development. These syndromes can affect multiple parts of the body, including the bones, muscles, skin, and internal organs.  
== Causes ==
== Causes ==
Overgrowth syndromes are typically caused by [[genetic mutation|mutations]] in various genes. These mutations can occur spontaneously (de novo) or they can be inherited from a parent. The specific genes involved vary depending on the particular syndrome. For example, [[Beckwith-Wiedemann syndrome]], one type of overgrowth syndrome, is often caused by changes in the genes on chromosome 11.
Overgrowth syndromes are typically caused by [[genetic mutation|mutations]] in various genes. These mutations can occur spontaneously (de novo) or they can be inherited from a parent. The specific genes involved vary depending on the particular syndrome. For example, [[Beckwith-Wiedemann syndrome]], one type of overgrowth syndrome, is often caused by changes in the genes on chromosome 11.
== Symptoms ==
== Symptoms ==
The symptoms of overgrowth syndromes can vary widely, but they often include increased height and weight, large body size, and other physical abnormalities. Some people with these syndromes may also have intellectual disabilities or developmental delays. Other symptoms can include [[macroglossia]] (an abnormally large tongue), [[organomegaly]] (enlarged organs), and [[hemihypertrophy]] (one side of the body being larger than the other).
The symptoms of overgrowth syndromes can vary widely, but they often include increased height and weight, large body size, and other physical abnormalities. Some people with these syndromes may also have intellectual disabilities or developmental delays. Other symptoms can include [[macroglossia]] (an abnormally large tongue), [[organomegaly]] (enlarged organs), and [[hemihypertrophy]] (one side of the body being larger than the other).
== Diagnosis ==
== Diagnosis ==
Diagnosis of overgrowth syndromes typically involves a physical examination, a review of the person's medical and family history, and genetic testing. [[Genetic testing]] can help identify the specific gene mutation causing the syndrome.
Diagnosis of overgrowth syndromes typically involves a physical examination, a review of the person's medical and family history, and genetic testing. [[Genetic testing]] can help identify the specific gene mutation causing the syndrome.
== Treatment ==
== Treatment ==
Treatment for overgrowth syndromes typically involves managing the symptoms and complications associated with the condition. This can include surgery to correct physical abnormalities, therapies to manage developmental delays, and regular monitoring for potential complications such as tumors.
Treatment for overgrowth syndromes typically involves managing the symptoms and complications associated with the condition. This can include surgery to correct physical abnormalities, therapies to manage developmental delays, and regular monitoring for potential complications such as tumors.
== See also ==
== See also ==
* [[Genetic disorder]]
* [[Genetic disorder]]
* [[Beckwith-Wiedemann syndrome]]
* [[Beckwith-Wiedemann syndrome]]
* [[Sotos syndrome]]
* [[Sotos syndrome]]
* [[Proteus syndrome]]
* [[Proteus syndrome]]
[[Category:Genetic disorders]]
[[Category:Genetic disorders]]
[[Category:Syndromes]]
[[Category:Syndromes]]

Latest revision as of 02:13, 4 April 2025


Overgrowth syndrome
Synonyms
Pronounce N/A
Specialty N/A
Symptoms Excessive growth, developmental delay, intellectual disability, macrocephaly, organomegaly
Complications Tumor development, cardiovascular abnormalities, orthopedic issues
Onset Prenatal or early childhood
Duration Lifelong
Types N/A
Causes Genetic mutation
Risks Family history, genetic predisposition
Diagnosis Clinical evaluation, genetic testing
Differential diagnosis Gigantism, Beckwith-Wiedemann syndrome, Sotos syndrome
Prevention None
Treatment Symptomatic treatment, surgical intervention
Medication
Prognosis Variable, depending on specific syndrome and complications
Frequency Rare
Deaths N/A


Overgrowth syndrome is a term used to describe a group of genetic disorders characterized by an increased growth rate, often resulting in an abnormally large size for a person's age or stage of development. These syndromes can affect multiple parts of the body, including the bones, muscles, skin, and internal organs.

Causes[edit]

Overgrowth syndromes are typically caused by mutations in various genes. These mutations can occur spontaneously (de novo) or they can be inherited from a parent. The specific genes involved vary depending on the particular syndrome. For example, Beckwith-Wiedemann syndrome, one type of overgrowth syndrome, is often caused by changes in the genes on chromosome 11.

Symptoms[edit]

The symptoms of overgrowth syndromes can vary widely, but they often include increased height and weight, large body size, and other physical abnormalities. Some people with these syndromes may also have intellectual disabilities or developmental delays. Other symptoms can include macroglossia (an abnormally large tongue), organomegaly (enlarged organs), and hemihypertrophy (one side of the body being larger than the other).

Diagnosis[edit]

Diagnosis of overgrowth syndromes typically involves a physical examination, a review of the person's medical and family history, and genetic testing. Genetic testing can help identify the specific gene mutation causing the syndrome.

Treatment[edit]

Treatment for overgrowth syndromes typically involves managing the symptoms and complications associated with the condition. This can include surgery to correct physical abnormalities, therapies to manage developmental delays, and regular monitoring for potential complications such as tumors.

See also[edit]




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