This Rare Rh Genotype ryr (CdE/cde) came originally from the Inca Indians in Andeans who brought all the up to the Aluets or Eskimos and Na-Dana Cree and Souix and then to Elamo-Dravidian in Persia and the Persian Parsis from Pars brought it to Karachi were Rh negative in 27% and B Rh negative with Rare Rh Genotype ryr (CdE/cde). I have this Rare Rh Genotype ryr. I got from my B Rh negative mother who came from Parsis in Karachi from Sassanian Noble family of Yazdegerd III daughter Nazbanu because it pass through the mother line. This is also Pure Atlantean from the Inca who some the originally Atlantean people, along with Mayans and Aztec but very few or the Mayan and Aztec had Rare Rh Genotype ryr (CdE/cde). unless the were Atlantean Royalty.
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:
: Study of an American Negro Family with the
: Rare Rh Genotype ryr (CdE/cde)
:
: Rare Rh Genotype ryr (CdE/cde)
: in Aluets or Eskimos and Incas in the
: Andeans have Rh Genotype ryr (CdE/cde)
:
: The highest frequency of an extremely
: rare r y (CdE) gene (=0.7%) in the Parsis is
: one of the most unique findings described
: so far in any population of the world. In
: Parsis it is poplymorphic whereas it is just
: sporadic in occurrence that too in a few
: populations only, the world over.
:
:
: The very rare Rh genotype Ryr (CdE/cde) in a
: case of erythroblastosis foetalis.
: Hemolytic disease of the newborn
: Main article: Hemolytic disease of the
: newborn
: The hemolytic condition occurs when there is
: an incompatibility between the blood types
: of the mother and the fetus. There is also
: potential incompatibility if the mother is
: Rh negative and the father is positive. When
: any incompatibility is detected, the mother
: receives an injection at 28 weeks gestation
: and at birth to avoid the development of
: antibodies toward the fetus. These terms do
: not indicate which specific antigen-antibody
: incompatibility is implicated. The disorder
: in the fetus due to Rh D incompatibility is
: known as erythroblastosis fetalis.
: • Hemolytic comes from two words:
: "hemo" (blood) and
: "lysis" (destruction) or breaking
: down of red blood cells
: • Erythroblastosis refers to the making of
: immature red blood cells
: • Fetalis refers to the fetus.
:
:
:
:
:
: The results at the Rh Locus in the Parsis
: have provided evidence for an orthodox
: nature
: of Rh gene “r” and a variable nature of R2
: gene. The highest frequency of an extremely
: rare r y (CdE) gene (=0.7%) in the Parsis is
: one of the most unique findings described
: so far in any population of the world. In
: Parsis it is poplymorphic whereas it is just
: sporadic in occurrence that too in a few
: populations only, the world over. The
: present
: analysis showed that founder’s principle
: i.e. genetic drift and a high degree of
: inbreeding
: among the early small number of migrants and
: subsequent cloning effect in successive
: generations have been responsible for such
: high ry gene complex among them. According
: to Morgan and Spuhler (1965), “in the
: absence of mutation, gene flow and
: selection, an
: idealized small population mating at random
: for a requisite number of generation (e.g.
: excluding negative assortative mating)
: dependent upon the size of the population,
: will
: reach a level of inbreeding equal to unity.”
: This may be true for early Parsi immigrants.
: Both size could not have been more than 100
: (?) people including men women and
: children and close relatives during 600-700
: A.D. Effective reproductive individuals will
: be still smaller. Parsis brought “ry” gene
: with hem since not a single example of “ry”
: has been reported from a vast literature
: available from India. “ry” gene and
: Heterosis:
: Some form of heterosis among the possessors
: of the “ry” gene complex appears plausible
: although difficult to prove, but the
: possibility cannot be excluded following
: Parson’s
: arguments. Parson (1962) while discussing
: “the initial increase of a new gene under
: positive assortative mating” came to the
: conclusion that “the condition under which
: new
: genes will increase in frequency under mixed
: positive asortative mating and random
: mating are discussed for populations in
: which two alleles are segregating at a
: locus.
: Whereas heterozygote advantage is essential
: under random mating for a new gene to
: become established, this is no longer a
: prerequisite with a proportion of
: assortative
: mating”. So far no specific selective
: advantage is known for “ry”.
: If any advantage is discovered them what
: Parsons (1963) thought of migration
: selection
: as an evolutionary factor may be as
: important as drift and viability differences
: between
: genotypes may be true for “ry” incidence
: among the Parsis. As a matter of fact
: Parsons
: has been looking forward for accurate
: unbiased data.
: “ry” gene complex appears to be of Iranian
: origin and it is strongly suspected that
: “ry” can
: still be detected in population groups from
: central Iran. The phenotype CeDEE reported
: by Sunderland and Smith (1966) could be ry
: R2 rather than R2 R2 as interpreted by them.
: Highest frequency in the world at HLA, A,B,
: and DR locus antigens and also in Gm
: and InV (1) loci can be explained on the
: basis of genetic drift in the small founder
: Parsi
: populations as mentioned which discussing
: “ry” story.
: Thus, the Rh system in the Parsis has
: provided evidences for genetic drift through
: “ry”
: selection through R2, and high degree of
: genetic stability though “r”.
:
:
:
:
:
: Erythroblastosis fetalis - Overview
: • Overview
: • Symptom
: • Treatment
: • Prevention
: • All Information
: Alternative Names
: Hemolytic disease of the newborn
: Definition of Erythroblastosis fetalis:
: Erythroblastosis fetalis is a potentially
: life-threatening blood disorder in a fetus
: or newborn infant. This article provides a
: general overview. For more detailed
: information see the specific disorder:
: • ABO incompatibility
: • Rh incompatibility
: Causes, incidence, and risk factors:
: Erythroblastosis fetalis develops in an
: unborn infant when the mother and baby have
: different blood types. The mother produces
: substances called antibodies that attack the
: developing baby's red blood cells.
: The most common form of erythroblastosis
: fetalis is ABO incompatibility, which can
: vary in severity.
: The less common form is called Rh
: incompatibility, which can cause very severe
: anemia in the baby.
:
: Source:
: http://www.umm.edu/ency/article/001298.htm#ixzz2ESaXmE8J
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