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1 Treatments  





2 References  





3 Further reading  





4 External links  














Dahlberg Borer Newcomer syndrome







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From Wikipedia, the free encyclopedia
 


Dahlberg Borer Newcomer syndrome
Other namesLymphedema hypoparathyroidism syndrome, Hypoparathyroidism lymphedema syndrome, Dahlberg syndrome.[1]

Dahlberg Borer Newcomer syndrome is a rare autosomal X-linked recessive genetic condition characterized by a prolapse of the bicuspid valve, progressive kidney failure, congenital lymphedema, hypoparathyroidism, and very short end bones of fingers.[2]

Treatments[edit]

Treatment for this condition is based on its symptoms. These treatments may include manual lymphatic drainage, consumption of beta blockersoranticoagulants for the bicuspid valve prolapse and vitamin Dorcalcium carbonate tablets for the hypoparathyroidism.[1]

References[edit]

  1. ^ a b "Lymphedema Hypoparathyroidism Syndrome". Lymphedema People. 2008-05-29. Archived from the original on 2012-05-05. Retrieved 2012-08-24.
  • ^ Dahlberg; et al. (September 1983). "Autosomal or X-linked recessive syndrome of congenital lymphedema, hypoparathyroidism, nephropathy, prolapsing mitral valve, and brachytelephalangy". American Journal of Medical Genetics. 16 (1): 99–104. doi:10.1002/ajmg.1320160115. PMID 6638075.
  • Further reading[edit]

    External links[edit]


    Retrieved from "https://en.wikipedia.org/w/index.php?title=Dahlberg_Borer_Newcomer_syndrome&oldid=1193639902"

    Category: 
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    This page was last edited on 4 January 2024, at 21:21 (UTC).

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