Kleinfelters is a chromosomal "trisomy" of the sex chromosomes. It is not inherited in a recessive or dominant manner.
There is no servant syndrome, It is likely that you are thinking albeit with bad spelling of Savant Syndrome. and it is recessive
Meckel Syndrome (type 1)is an autosomal recessive trait carried on chromosome 17.
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.
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.
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.
Zellweger syndrome is autosomal recessive.
Cockayne syndrome is a recessive trait.
It is recessive
recessive
There is no servant syndrome, It is likely that you are thinking albeit with bad spelling of Savant Syndrome. and it is recessive
is restless leg syndrome dominant or recessive
Dont be dumb It's clearly 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.
It is a recessive X linked form of muscular dystrophy
Nondisjunction in males can lead to disorders such as Klinefelter syndrome, where individuals have an extra X chromosome (XXY) instead of the typical XY combination. This can result in symptoms like reduced fertility, gynecomastia, and developmental delays.
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.