autosomal dominant is only when one allele is messed up
autosomal recessive is when you give the disease to your child 50/50 chance.
Not true.... 50/50 when its Autosomal Dominant(see below)
Both parents carry a normal gene (N), and a faulty, recessive, gene (n). The parents, although carriers, are unaffected by the faulty gene. Their offspring are affected, not affected, or carriers. This type of inheritance was first shown by Mendel.
One parent has a single, faulty dominant gene (D), which overpowers its normal counterpart (d), affecting that parent. When the affected parent mates with an unaffected and non-carrier mate (dd), the offspring are either affected or not affected, but they are not carriers.
An autosomal genetic disorder is Huntington's disease.
Progressive Retina Atrophy is a dominant genetic disorder.
1. Shape of face (probably polygenic) Oval dominant, square recessive 2. Cleft in chin No cleft dominant, cleft recessive 3. Hair curl (probably polygenic) Assume incomplete dominance Curly: homozygous Wavy: heterozygous Straight: homozygous 4. Hairline Widow peak dominant, straight hairline recessive 5. Eyebrow size Broad dominant, slender recessive 6. Eyebrow shape Separated dominant, joined recessive 7. Eyelash length Long dominant, short recessive 8. Dimples Dimples dominant, no dimples recessive 9. Earlobes Free lobe dominant, attached recessive 10. Eye shape Almond dominant, round recessive 11. Freckles Freckles dominant, no freckles recessive 12. Tongue rolling Roller dominant, nonroller recessive 13. Tongue folding Inability dominant, ability recessive 14. Finger mid-digital hair Hair dominant, no hair recessive 15. Hitch-hiker's thumb Straight thumb dominant, hitch-hiker thumb recessive 16. Bent little finger Bent dominant, straight recessive 17. Interlaced fingers Left thumb over right dominant, right over left recessive 18. Hair on back of hand Hair dominant, no hair recessive 19. Tendons of Palmar Muscle Two tendons dominant, three tendons recessive
Anyone can be a carrier of a recessive genetic disorder (as long as it is not associated with the sex chromosomes) no matter what their gender since "carrier" refers to an individual that is heterozygous for the recessive allele and therefore phenotypically normal. Specifically, sexlinked genetic disorders can be "carried" by a heterozygous female but males (having only one X chromosome) cannot. Males will either be free of the defective gene or be affected.
how is it possible for a person to have dominant genetic disorder? how is it possible for a person to have dominant genetic disorder?
It is autosomal recessive and it is not a disorder! Cystic Fibrosis is a disease.
Sickle cell anemia is an autosomal recessive disorder. It can result from two carriers having a child together.
No, cystic fibrosis is an autosomal recessive disorder.
Autosomal dominant, Autosomal recessive, X-linked recessive and X-linked dominant
autosomal dominant
hey I'm not positive but I believe that Cystic Fibrosis is autosomal. My reasonning for this is that there seems to be an equal number of females that have cystic fibrosis as there are males. I AM NOT POSITIVE.
Autosomal dominant Autosomal recessive X linked recessive.
Autosomal dominant Autosomal recessive X linked recessive.
I think I read somewhere that there are some variants of it that are recessive and others that are dominant.
It is an autosomal recessive trait.
yes it is, only 1 mutation to the lmna gene is sufficent for someone to express traits regarding progeria
the disorder is usually either autosomal recessive or autosomal dominant. they are passed down from the parents to the next generation. autosomal reccessive diseases only are when one parent gives one reccessive allele and the other parent gives the other reccessive allele. A dominant autosomal disorder can be inherited with one or two of the alleles.