Rett syndrome is a rare genetic disorder that is typically caused by a mutation in the MECP2 gene located on the X chromosome. It is not classified as dominant or recessive in the traditional sense because it primarily affects individuals with two X chromosomes. It is considered an X-linked dominant disorder with variable expressivity and reduced penetrance.
There is no servant syndrome, It is likely that you are thinking albeit with bad spelling of Savant Syndrome. and it is recessive
Kleinfelters is a chromosomal "trisomy" of the sex chromosomes. It is not inherited in a recessive or dominant manner.
Lobster claw syndrome, or Ectrodactyly, is a rare genetic condition caused by a mutation in the TP63 gene, which is inherited in an autosomal dominant pattern. This means that only one copy of the mutated gene is needed to display the syndrome.
Cat eye syndrome is a genetic condition that is caused by an extra piece of genetic material on chromosome 22. It is not determined by simple dominant or recessive inheritance patterns, but rather by the presence of the extra genetic material.
There are several causes of Anglemann syndrome. None of them are inherited as a dominant recessive or co-dominant characteristics. The most common cause (68% of cases) is a deletion of the q12 region of the maternally derived chromosome 15.
It is recessive
recessive
Zellweger syndrome is autosomal recessive.
is restless leg syndrome dominant or recessive
Cockayne syndrome is a recessive trait.
There is no servant syndrome, It is likely that you are thinking albeit with bad spelling of Savant Syndrome. and it is recessive
semi-dominant--semi-recessive
Down syndrome is neither dominant nor recessive. Actually, it is considered to be an "autosomal" trait. This occurs when there is damage to the chromosome.
Dominant and recessive
Down syndrome is neither caused by dominant or recessive chromosomes it is simply caused by an error in the translation process of chromosome 21.
Dont be dumb It's clearly recessive
Rett syndrome in boys is known as Rett syndrome. Male fetuses with Rett syndrome do not typically survive until birth unless they have an extra X chromosome (XXY).