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How is DiGeorge syndrome diagnosed?
Diagnosis of DiGeorge syndrome can be made by ultrasound examination around the eighteenth week of pregnancy, when abnormalities in the development of the heart or the palate can be detected.
What is the treatment for digeorge syndrome?
Children with DiGeorge syndrome should be kept on low-phosphorus diets and kept away from crowds or other sources of infection. They should not be immunized with vaccines made from live viruses or given corticosteroids.
What other name does DiGeorge syndrome go by?
DiGeorge syndrome (also called 22q11 deletion syndrome, congenital thymic hypoplasia, or third and fourth pharyngeal pouch syndrome)
How many babies with tetralogy of fallot have digeorge syndrome?
I'm not sure how many children with tetralogy of fallot have digeorge however my son has tetralogy of fallot repaired in 2006. He also has a partial deletion of chromosome 22 DiGeorge Syndrome. He is doing really well and his speech/articulation is emerging.
Why do people laugh and make fun of people with digeorge syndromee i have digeorge syndrome and evryone at school either dislikes me or laughs at me why is that?
this a phenmon of picking on the weak. I have dyslexia and ADD so i get bullied. your not alone.
What is the type of mutation that causes Digeorge syndrome?
Deletion Mutation causes DiGeorges Syndrome.
Were people with digeorge syndrome mistreated in the past?
This is an interesting question! We've notified our experts in this category and we'll email you when there is a response.
What do nude mice and humans and with digeorge's syndrome have in common?
They have something that they really have...
How prevalent is DiGeorge syndrome?
estimates range from 1:4000 to 1:6395.
What part of the body does digeorge syndrome?
DiGeorge syndrome affects multiple systems in the body, but it is primarily associated with developmental issues in the immune system and the heart. It is caused by a deletion on chromosome 22 and can lead to a range of symptoms including heart defects, immune system deficiencies, and developmental delays.
What are the symptoms of DiGeorge syndrome?
The disorder is marked by absence or underdevelopment of the thymus and parathyroid glands.
Is digeorge syndrome dominant autosomal or sex-linked?
DiGeorge syndrome is not caused by a single gene mutation, but rather by a deletion of a portion of chromosome 22. It is not inherited in a simple Mendelian pattern like dominant autosomal or sex-linked traits.
