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Is cat eye syndrome dominant or recessive?
autosomal dominant.......... i think
How do you detect if you have down syndrome?
Autosomal means that it concerns an autosome--a chromosome other than a sex chromosome. Down syndrome is caused by an additional copy of the 21st chromosome. Since the 21st chromosome is not a sex chromosome, Down syndrome is autosomal.
What chromosome is affected by meckel syndrome?
Meckel Syndrome (type 1)is an autosomal recessive trait carried on chromosome 17.
Turner syndrome its autosomal?
No. It is sex linked, of a sort. The female is born with one X chromosome.
How any chromosomes are in each human cell?
If you mean how many; there are 46, or 23 homologous pairs. There are 22 autosomal pairs and the sex chromosomes (X and X/Y). This can vary in some disorders, such as Down Syndrome, Turner Syndrome, Klinefelter's Syndrome, and Triple X Syndrome.
How do you get Apert syndrome?
Apert syndrome is a genetic defect, so that means that the child will have it from conception (it's an autosomal dominant genetic defect, which means that only one parent needs to supply the defective gene in order for the child to be born with it.)
Is apert syndrome dominant or recessive?
Recessive, but dominant in some rare cases.
Is sickle cell anemia a sexlinked trait?
Nope! The disease is equally in both males and females. This means that it is autosomal.
What is syndactyly a symptom of?
Syndactyly is a characteristic of Apert syndrome, Poland syndrome, Jarcho-Levin syndrome, oral-facial-digital syndrome, Pfeiffer syndrome, and Edwards syndrome
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 other conditions could an infant with syndactyly have?
Syndactyly is a characteristic of Apert syndrome, Poland syndrome, Jarcho-Levin syndrome, oral-facial-digital syndrome, Pfeiffer syndrome, and Edwards syndrome.
Is Zellweger syndrome dominant or recessive?
Zellweger syndrome is autosomal recessive.
When was Apert syndrome first discovered?
Apert Syndrome was first discovered by a French Physician named Eugene Apert in 1906 when he described nine different individuals with common characteristics and attributes.These patients were suffering from acrocephalosyndactyly, wherein the bone or skin between the toes and fingers fuses together because no selective cell death is taking place.
Is marfan syndrome automsomal dominant?
Yes, Marfan syndrome is autosomal dominant.
Is cri du chat syndrome autosomal?
Yes.Autosomal deletion syndrome affecting chromosome 5..
Is Edwards syndrome autosomal or sex linked?
Google has the answer for everything.
Is klinefelters syndrome autosomal or x- linked?
X-linked
