X-linked
Autosomal dominant, Autosomal recessive, X-linked recessive and X-linked dominant
X Linked
Turner syndrome is a condition that affects females and is caused by a missing or incomplete X chromosome. It is considered an autosomal condition because it is located on one of the non-sex chromosomes, specifically the X chromosome.
No
Klinefelter Syndrome is sex-linked, because it is a genetic defect that results in a male having an extra X chromosome.
Turner syndrome is not autosomal; rather, it is caused by a complete or partial absence of one of the X chromosomes in females, resulting in a monosomy (45,X). This chromosomal condition can lead to various physical and developmental features, such as short stature and infertility.
Marfan syndrome is caused by a mutation in the FBN1 gene, which is located on chromosome 15 and is inherited in an autosomal dominant pattern. It is not linked to the X chromosome. Both males and females can inherit and display symptoms of Marfan syndrome.
Inheritance syndrome is typically inherited in an autosomal dominant pattern, meaning that a mutation in one copy of the affected gene is enough to cause the syndrome. This means that an affected individual has a 50% chance of passing the syndrome on to their offspring. Rarely, inheritance syndrome can also be inherited in an autosomal recessive or X-linked pattern.
Autosomal dominant Autosomal recessive X linked recessive.
Autosomal dominant Autosomal recessive X linked recessive.
"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.
No. People with Klinefelter's syndrome have a normal Y chromosome and 2 normal X chromosomes.