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Results 1 - 10 of 24 for Feingold syndrome
  1. Feingold syndrome is a disorder that affects many parts of the body. There are two types of Feingold syndrome, distinguished by their genetic cause; both types ...
  2. ... the MYCN gene have been found to cause Feingold syndrome type 1. This developmental disorder is characterized by ... for making the protein. In some cases of Feingold syndrome type 1, the entire MYCN gene is deleted. ...
  3. ... reduce the amount of the MIR17HG gene cause Feingold syndrome type 2. This developmental disorder is characterized by ... the problems with growth and development characteristic of Feingold syndrome type 2, it remains unclear exactly how a ...
  4. ... leading to cancer. More About This Health Condition Feingold syndrome type 2 is caused by genetic changes that ... These changes are known as 13q31.3 microdeletions. Feingold syndrome type 2 is characterized by abnormalities of the ...
  5. Hand Injuries and Disorders (National Library of Medicine)  
    No matter how old you are or what you do for a living, you are always using your hands. When there is something wrong with them, you may not be able to ...
  6. Foot Injuries and Disorders (National Library of Medicine)  
    Each of your feet has 26 bones, 33 joints, and more than 100 tendons, muscles, and ligaments. No wonder a lot of things can go wrong. Here are a few common ...
  7. Intestinal Obstruction (National Library of Medicine)  
    An intestinal obstruction occurs when food or stool cannot move through the intestines. The obstruction can be complete or partial. There are many causes. ...
  8. Facts about Down Syndrome (Centers for Disease Control and Prevention)  
    Down Syndrome/Start Here ... Down Syndrome ... Centers for Disease Control and Prevention ... Down syndrome is a condition in which a person has an extra chromosome. ...
  9. ... 1399-0004.1980.tb00126.x. Citation on PubMed Feingold M, Sklower SL, Willner JP, Desnick RH, Cohen MM. Craniosynostosis-radial aplasia: Baller-Gerold syndrome. Am J Dis Child. 1979 Dec;133(12): ...
  10. ... Hachem JP, Behne M, Moskowitz DG, Christiano AM, Feingold KR, Elias PM. Structural and functional consequences of loricrin mutations in human loricrin keratoderma (Vohwinkel syndrome with ichthyosis). J Invest Dermatol. 2004 Apr;122( ...
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