This is an X linked disease
Lowe syndrome is caused by a mutated gene on the X sex chromosome. Because it is X-linked, it occurs almost exclusively in males.
WAS is inherited as an X-linked genetic disorder and will therefore only affect males.
Yes, Fragile X syndrome is an X-linked genetic disorder that causes a range of developmental problems. It is caused by a mutation in the FMR1 gene located on the X chromosome. The condition is more commonly seen in males than in females because they have only one X chromosome.
Lowe's Syndrome is a rare X-linked recessive disorder. This means that the gene is on the X chromosome. Girls can carry this gene but since they have 2 X chromosomes, it is not expressed in them but carried by them. It is seen in boys since they have one X and one Y. They do not have a second X to "hide" the gene. See more information at the link below:
One disorder could be colorblindness. Colorblindness is most common in males because in order to have to disorder you must carry two mutated X chromosomes. Another recessive genetic disorder you can get is called Hemophilia. This is a disorder in which the genes for hemoglobin are not present and your body is not able to create blood clots and a simple scratch can be very serious.
X-linked
Klinefelter Syndrome is sex-linked, because it is a genetic defect that results in a male having an extra X chromosome.
Lowe syndrome is caused by a mutated gene on the X sex chromosome. Because it is X-linked, it occurs almost exclusively in males.
I think it's dominant because when you have sex you are sharing your love.
It is a recessive X linked form of muscular dystrophy
The syndrome is caused by a severe change (mutation) in the HPRT gene . Since the HPRT gene is located on the X chromosome, Lesch-Nyhan syndrome is considered an X-linked disorder and therefore only affects males.
WAS is inherited as an X-linked genetic disorder and will therefore only affect males.
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.
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.
WAS is inherited as an X-linked genetic disorder and will therefore only affect males.
Tourette's syndrome is not classified as an X-linked disease; rather, it is considered a complex neurodevelopmental disorder with a multifactorial inheritance pattern. While genetic factors play a significant role in its development, it is influenced by both genetic and environmental factors. Some studies suggest a potential link to specific genes, but these are not strictly tied to the X chromosome. Therefore, the inheritance of Tourette's syndrome does not follow the typical patterns of X-linked disorders.
Three disorders which are sex-linked are: Fragile X syndrome Duchenne muscular dystrophy Colour blindness (most forms, but not all)