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What else can I help you with?
Is progeria autosomal?
yes it is, only 1 mutation to the lmna gene is sufficent for someone to express traits regarding progeria
Is progeria a recessive or dominant disorder?
yes it is, only 1 mutation to the lmna gene is sufficent for someone to express traits regarding progeria
Is progeria autosomal or sex-linked?
Progeria is neither autosomal nor sex-linked. It is caused by a spontaneous mutation in the LMNA gene, which is located on chromosome 1.
Is progeria a dominant or recessive gene?
progeria is recessive, that's an easy question, dont be dumbactually progeria is dominant, according to the Progeria Research Foundation
What is the chromosomal locus of progeria?
Progeria causes you to have missing chromosomes in your body function
What is the progeria for karyotype?
Progeria, specifically Hutchinson-Gilford Progeria Syndrome (HGPS), is a rare genetic disorder caused by a mutation in the LMNA gene, which encodes the protein lamin A. This condition leads to accelerated aging in children, characterized by symptoms such as growth failure, hair loss, joint stiffness, and cardiovascular issues. The karyotype of individuals with progeria is typically normal, with no chromosomal abnormalities, but the mutation affects the structure and function of the lamin A protein, leading to the disease's symptoms.
What is the common name for Progeria?
Anageria is the medical term for Progeria. There is a thread in the sci.med group discussing this way back in '95, but the poster never published a follow-up, I think.
What is the environmental factor that causes the mutation on the LMNA gene to cause Progeria?
nuclear waste dumped into water supply
What individuals catch progeria?
how many individuals get the progeria? Progeria is a very rare genetic disease and can't be "caught." You are either born with it or not. If you are not born with it, you can never develop it. The incidence of progeria is about 1 in every 8 million live births.
Who are most likely to get progeria male or female?
Progeria, specifically Hutchinson-Gilford Progeria Syndrome (HGPS), affects both males and females equally, with no significant difference in prevalence between the two genders. The condition is caused by a mutation in the LMNA gene, which occurs randomly and is not linked to sex. Therefore, both male and female infants are at the same risk of developing progeria.
Is progeria non disjunction?
No, progeria is not caused by non disjunction. Progeria is a rare genetic disorder where a mutation occurs in the LMNA gene, leading to premature aging in children. Non disjunction is a different type of genetic error where chromosomes fail to separate properly during cell division.
Where can a punnett square for progeria be found?
A Punnett square is a tool used in genetics to predict the likelihood of certain traits being passed on from parents to offspring. Progeria is a rare genetic disorder characterized by accelerated aging in children. A Punnett square for progeria would not be relevant as it is not a trait that follows typical Mendelian inheritance patterns.
