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    Topic review

    Bowen-Conradi Syndrome

    Subjects: Genetics
    View times: 3
    Submitted by: Catherine Yang
    (This entry belongs to Entry Collection "MedlinePlus ")

    Definition

    Bowen-Conradi syndrome is a disorder that affects many parts of the body and is usually fatal in infancy. Affected individuals have a low birth weight, experience feeding problems, and grow very slowly. Their head is unusually small overall (microcephaly), but is longer than expected compared with its width (dolichocephaly). Characteristic facial features include a prominent, high-bridged nose and an unusually small jaw (micrognathia) and chin. Affected individuals typically have pinky fingers that are curved toward or away from the ring finger (fifth finger clinodactyly) or permanently flexed (camptodactyly), feet with soles that are rounded outward (rocker-bottom feet), and restricted joint movement.

    1. Introduction

    Other features that occur in some affected individuals include seizures; structural abnormalities of the kidneys, heart, brain, or other organs; and an opening in the lip (cleft lip) with or without an opening in the roof of the mouth (cleft palate). Affected males may have the opening of the urethra on the underside of the penis (hypospadias) or undescended testes (cryptorchidism).

    Babies with Bowen-Conradi syndrome do not achieve developmental milestones such as smiling or sitting, and they usually do not survive more than 6 months.

    2. Frequency

    Bowen-Conradi syndrome is common in the Hutterite population in Canada and the United States; it occurs in approximately 1 per 355 newborns in all three Hutterite sects (leuts). A few individuals from outside the Hutterite community with signs and symptoms similar to Bowen-Conradi syndrome have been described in the medical literature. Researchers differ as to whether these individuals have Bowen-Conradi syndrome or a similar but distinct disorder.

    3. Causes

    Bowen-Conradi syndrome is caused by a mutation in the EMG1 gene. This gene provides instructions for making a protein that is involved in the production of cellular structures called ribosomes, which process the cell's genetic instructions to create new proteins. Ribosomes are assembled in a cell compartment called the nucleolus.

    The particular EMG1 gene mutation known to cause Bowen-Conradi syndrome is thought to make the protein unstable, resulting in a decrease in the amount of EMG1 protein that is available in the nucleolus. A shortage of this protein in the nucleolus would impair ribosome production, which may reduce cell growth and division (proliferation); however, it is unknown how EMG1 gene mutations lead to the particular signs and symptoms of Bowen-Conradi syndrome.

    4. Inheritance

    This condition is inherited in an autosomal recessive pattern, which means both copies of the gene in each cell have mutations. The parents of an individual with an autosomal recessive condition each carry one copy of the mutated gene, but they typically do not show signs and symptoms of the condition.

    5. Other Names for This Condition

    • Bowen Hutterite syndrome
    • Bowen syndrome, Hutterite type
    • Bowen-Conradi Hutterite syndrome
    • BWCNS
    • Hutterite syndrome

    The entry is from https://medlineplus.gov/genetics/condition/bowen-conradi-syndrome

    References

    1. Armistead J, Khatkar S, Meyer B, Mark BL, Patel N, Coghlan G, Lamont RE, LiuS, Wiechert J, Cattini PA, Koetter P, Wrogemann K, Greenberg CR, Entian KD,Zelinski T, Triggs-Raine B. Mutation of a gene essential for ribosome biogenesis,EMG1, causes Bowen-Conradi syndrome. Am J Hum Genet. 2009 Jun;84(6):728-39. doi: 10.1016/j.ajhg.2009.04.017.
    2. Armistead J, Patel N, Wu X, Hemming R, Chowdhury B, Basra GS, Del Bigio MR,Ding H, Triggs-Raine B. Growth arrest in the ribosomopathy, Bowen-Conradisyndrome, is due to dramatically reduced cell proliferation and a defect inmitotic progression. Biochim Biophys Acta. 2015 May;1852(5):1029-37. doi:10.1016/j.bbadis.2015.02.007.
    3. Armistead J, Triggs-Raine B. Diverse diseases from a ubiquitous process: theribosomopathy paradox. FEBS Lett. 2014 May 2;588(9):1491-500. doi:10.1016/j.febslet.2014.03.024.
    4. Lamont RE, Loredo-Osti J, Roslin NM, Mauthe J, Coghlan G, Nylen E, Frappier D,Innes AM, Lemire EG, Lowry RB, Greenberg CR, Triggs-Raine BL, Morgan K, WrogemannK, Fujiwara TM, Zelinski T. A locus for Bowen-Conradi syndrome maps to chromosomeregion 12p13.3. Am J Med Genet A. 2005 Jan 15;132A(2):136-43.
    5. Lowry RB, Innes AM, Bernier FP, McLeod DR, Greenberg CR, Chudley AE, ChodirkerB, Marles SL, Crumley MJ, Loredo-Osti JC, Morgan K, Fujiwara TM. Bowen-Conradisyndrome: a clinical and genetic study. Am J Med Genet A. 2003 Jul30;120A(3):423-8.
    6. Sondalle SB, Baserga SJ. Human diseases of the SSU processome. Biochim BiophysActa. 2014 Jun;1842(6):758-64. doi: 10.1016/j.bbadis.2013.11.004.
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