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Q: What cromasome is affected by scid?
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Horses that were born with the SCID virus have what?

Foals with severe combined immunodeficiency (SCID) are born with severely weakened immune systems. SCID is an autosomal recessive inherited condition identified in Arabian and part-Arabian horses. Affected foals are highly susceptible to infections from which they cannot recover. Answer From: BlueHorse211


How many people are affected by severe combined immunodeficiency?

SCID is thought to affect between one in every 100,000 persons, and one in every 500,000 infants. Children with SCID are vulnerable to recurrent severe infections, retarded growth, and early death.


Who discovered scid?

John handcock discoverer scid in 1678


What is SCID with leukopenia?

SCID with leukopenia. Children with this form of SCID are lacking a type of white blood cell called a granulocyte.


How can you tell if your horse has SCID?

If your horse has SCID it will be dead, but if it carries SCID you can only find out be having your horse's blood tested. This is only important in breeding stock, usually only stallions, but generally required in mares if you are going to breed to a SCID tested positive stallion.


On howrse horses born with the SCID virus have?

horses born with the scid virus have on howrse


How many cases of SCID are autosomal recessive?

About 40% of SCID cases are inherited from the parents in an autosomal recessive pattern.


How many causes of SCID are adenosine deaminase deficiency?

Adenosine deaminase deficiency (ADA). About 50% of SCID cases are of this type.


What are the categories of SCID?

Several different immune system disorders are currently grouped under SCID: Swiss-type agammaglobulinemia. Adenosine deaminase deficiency (ADA). Autosomal recessive. Bare lymphocyte syndrome. SCID with leukopenia


Are there any famous people that have scid?

me


What are treatments for SCID?

Patients with SCID can be treated with antibiotics and immune serum to protect them from infections. Bone marrow transplants are currently regarded as one of the few effective standard treatments for SCID. In 1990, the.(FDA) approved PEG-ADA.


What is the prognosis of scid?

Most people who are diagnosed with SCID are very young because SCID is inherited genetically from parents. If a patient is untreated when they have SCID, they could die before the age of 1 or 2. A treatment for SCID is transplanting blood-forming stem cells in bone marrow. It is most effective if there is a matching brother or sister willing to donate blood marrow, and has the most success if done before the first 3 months of life.