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April Letters

Readers respond to the February Issue

  • Smithsonian magazine, April 2006

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    Most Popular

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    1. Gobekli Tepe: The World’s First Temple?
    2. Tattoos
    3. The Coldest Place in the Universe
    4. The 'Secret Jews' of San Luis Valley
    5. A Brief History of the Salem Witch Trials
    6. John Hodgman Gives “More Information Than You Require”
    7. America's First True "Pilgrims"
    8. New Light on Stonehenge
    9. One Man's Korean War
    10. Family Ties
    1. Gobekli Tepe: The World’s First Temple?
    2. The 'Secret Jews' of San Luis Valley
    3. Sarah Vowell on the Puritans' Legacy
    4. Bugs, Brains and Trivia
    5. The Coldest Place in the Universe
    6. America's First True "Pilgrims"
    7. The Financial Panic of 1907: Running from History
    8. Munich at 850
    9. Jukebox: A Choir of Turkeys
    10. Inside Iran's Fury

    Genetic Misconceptions

    "Medical Sleuth," about Dr. D. Holmes Morton’s work with genetic diseases among Amish and Mennonite people in Pennsylvania, prompted many readers to ask why such communities do not avail themselves of premarital or prenatal genetic screening to prevent the birth of afflicted children.

    Dr. Morton responds:
    When the Plain people, which include the Amish and Mennonite, came to Lancaster County from Europe about 300 years ago, they carried a set of recessive gene mutations that are still present in U.S. and European populations. As the two Plain populations expanded from 20 to 50 founding couples to 20,000 to 50,000 people, some recessive mutations became more common, while other genes became less common or even disappeared. The change in gene mutation frequencies within a new, small, rapidly expanding population is called “random genetic drift,” and it—not inbreeding or natural selection—is the major reason for the high incidence of specific recessive disorders in isolated human populations, including the Plain communities. Over the same period, genetic drift has also been at work within the U.S. general population. As a result, cystic fibrosis is a very common recessive disorder in the U.S. Caucasian population, but is absent in the Plain populations of Lancaster County. The carrier rate for this disorder is now 1 in 25 people, 4,000 per 100,000 in the general U.S. population.

    Contrary to popular belief, preventing the birth of children with recessive genetic disorders, or allowing affected infants to die from lack of medical care, does not significantly decrease the disease risk in a population over time. That’s because the risk of genetic disease in a population resides in carriers, rather than in a few affected children who have two copies of the abnormal gene.

    For the Plain people, prearranged marriages and therapeutic abortions are not acceptable. But they have readily taken advantage of genetic testing and expanded newborn screening for certain inherited disorders, because successful treatment usually depends on early detection and prevention of severe illnesses.

    Our clinic seeks to improve methods of diagnosing and treating genetic disorders in the Plain communities. An understanding that many common medical problems arise from genetic causes and are nonetheless treatable may prove to be an important contribution of the Plain people to modern medicine.

    D. Holmes Morton, M.D.
    Clinic for Special Children
    Strasburg, Pennsylvania

    Bahamian Blenny

    1 2

    Genetic Misconceptions

    "Medical Sleuth," about Dr. D. Holmes Morton’s work with genetic diseases among Amish and Mennonite people in Pennsylvania, prompted many readers to ask why such communities do not avail themselves of premarital or prenatal genetic screening to prevent the birth of afflicted children.

    Dr. Morton responds:
    When the Plain people, which include the Amish and Mennonite, came to Lancaster County from Europe about 300 years ago, they carried a set of recessive gene mutations that are still present in U.S. and European populations. As the two Plain populations expanded from 20 to 50 founding couples to 20,000 to 50,000 people, some recessive mutations became more common, while other genes became less common or even disappeared. The change in gene mutation frequencies within a new, small, rapidly expanding population is called “random genetic drift,” and it—not inbreeding or natural selection—is the major reason for the high incidence of specific recessive disorders in isolated human populations, including the Plain communities. Over the same period, genetic drift has also been at work within the U.S. general population. As a result, cystic fibrosis is a very common recessive disorder in the U.S. Caucasian population, but is absent in the Plain populations of Lancaster County. The carrier rate for this disorder is now 1 in 25 people, 4,000 per 100,000 in the general U.S. population.

    Contrary to popular belief, preventing the birth of children with recessive genetic disorders, or allowing affected infants to die from lack of medical care, does not significantly decrease the disease risk in a population over time. That’s because the risk of genetic disease in a population resides in carriers, rather than in a few affected children who have two copies of the abnormal gene.

    For the Plain people, prearranged marriages and therapeutic abortions are not acceptable. But they have readily taken advantage of genetic testing and expanded newborn screening for certain inherited disorders, because successful treatment usually depends on early detection and prevention of severe illnesses.

    Our clinic seeks to improve methods of diagnosing and treating genetic disorders in the Plain communities. An understanding that many common medical problems arise from genetic causes and are nonetheless treatable may prove to be an important contribution of the Plain people to modern medicine.

    D. Holmes Morton, M.D.
    Clinic for Special Children
    Strasburg, Pennsylvania

    Bahamian Blenny

    I share Gordon Chaplin’s concern about the degradation of Bahamian reef systems (“A Return to the Reefs”). In fact, in 1956, while working on my PhD dissertation, I visited James E. Böhlke at the Academy of Natural Sciences in Philadelphia when he was collaborating with the author’s father, Charles C.G. Chaplin, on the book Fishes of the Bahamas. Böhlke generously made available their collections, and I even named a species of blenny after him, Malacoctenus boehlkei.
    Victor G. Springer
    National Museum of Natural HIstory
    Washington, D.C.

    Lesson Learned?

    David Von Drehle (“A Lesson in Hate”) hauls out the cliché “Why do they hate us?” and says jihad theorist Sayyid Qutb and his disciples were “insane.” This is hardly helpful in broadening our understanding of the crisis. The real answer can be found earlier in the article: “Western powers were creating, with absolute colonial confidence, new maps and governments for the Middle East. For a proud man like Sayyid Qutb, the humiliation of his country at the hands of secular leaders and Western puppets was galling.” Yet Von Drehle emphasizes that Qutb, and thus many citizens of the region today, “hate us” because of our haircuts.
    Rob Riley
    Chicago, Illinois

    My grandfather Henry “Hank” Croissant owned a barbershop in Greeley, Colorado, from the ’40s until his death in the mid ’60s, and he surely must have cut Sayyid Qutb’s hair. Hank loved his country, his family, his life and everything about Greeley. My grandfather was everything Qutb wasn’t.
    Chris Pedersen
    Bedford, New Hampshire


     
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