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What else can I help you with?
What is the life expectancy of someome with robinow syndrome?
Life expectancy can vary for individuals with Robinow syndrome depending on the severity of their symptoms and associated complications. In general, most individuals with Robinow syndrome have a normal lifespan, but some may experience health issues that can affect their life expectancy. It is important for individuals with Robinow syndrome to receive regular medical monitoring and appropriate care to manage their condition.
Is Angelman Syndrome more common in males or females?
From what I found, they are both equally common.
Does Angelman syndrome affect people of certain ethnic origins?
Angelman syndrome can affect people of any ethnic background. It is caused by a genetic mutation on chromosome 15 and can occur in individuals regardless of their ethnic origins.
Are there any famous people with Angelman Syndrome?
The sons of actor Colin Farrell, author Ian Rankin, professional baseball player Dave Henderson and professional hockey player Peter McDuffe. No other truly famous people have been diagonsed with this condition as far as i know. Hope that helped :)
What is the life expectancy for a child with Bardet-Biedl syndrome?
Life expectancy for individuals with Bardet-Biedl syndrome can vary greatly depending on the severity of their symptoms and medical management. Many individuals with this syndrome can live into adulthood with appropriate medical care and monitoring. However, complications associated with the syndrome, such as obesity-related issues and kidney problems, can impact life expectancy.
Who identified Angelman syndrome?
in 1965 Harry Angelman
Is Angelman syndrome the same as Down syndrome?
Angelman syndrome is a genetic disorder, as is Down syndrome. But they are not the same. Angelman Syndrome involves a deletion of Chromosome 15, whereas people with Down syndrome have an extra copy of Chromosome 21.
How long do people with angelman syndrome live for?
People with Angelman Syndrome usually have a normal life span unless they have it severe or a bad rare kind of it. This can be followed up by looking for the symptoms.
Do black people have angelman syndrome?
Yes. All races and both males and females get Angelman Syndrome.
What is Angelman's Syndrome's scientific name?
Angelman syndrome's scientific name is "AS," or "Angelman syndrome." It is a genetic disorder characterized by developmental delays, speech impairments, and unique behaviors. It is caused by a loss of function in a specific gene located on chromosome 15.
What percentage of babies is born with Angelman syndrome?
One out of 20,000 babbies are born with angelman syndrome.
What is the life expectancy of a patient with Marfan syndrome?
Recent advances in Marfan syndrome treatment have prolonged the life expectancy of patients considerably. Changes in how the syndrome is treated, including medication, surgical interventions, and monitoring for complications of the syndrome (eg, aneurysms), are all responsible for the increase in life expectancy. The prolongation in life expectancy can be seen by taking a look at statistics from 1972, in which the life expectancy was 32 years, and from 1996, where patients with Marfan syndrome had a life expectancy of 61 years.
Angelman syndrome effects gender and ethnicity?
no
Is angelman syndrome a recessive or a dominant?
It is recessive
Is angelman syndrome autosomal?
"Autosomal" means the syndrome or disorder of interest is pertaining to a chromosome that is not a sex chromosome, either X or Y. Angelman and Prader-Willi Syndrome are both caused by a deletion (or disruption of a gene) on chromosome 15, which is an autosomal chromosome and not a sex chromosome. Therefore, yes, Angelman syndrome is considered an autosomal syndrome.
What organisms are used in researching angelman syndrome and how are they used?
Mice and humans are used in researching Angelman Syndrome. In mice, the condition is genetically induced, and then a medical trial treatment is applied. In humans, previously approved treatments for other illnesses are used on individuals that were born with Angelman Syndrome.
What is the life expectancy for prune belly syndrome?
a good long life
