Dahlberg Borer Newcomer syndrome

Other names| Lymphedema 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]

## Contents

* 1 Treatments
* 2 References
* 3 Further reading
* 4 External links

## Treatments

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

## References

1. ↑ 1.0 1.1 "Lymphedema Hypoparathyroidism Syndrome". Lymphedema People. 2008-05-29. http://www.lymphedemapeople.com/thesite/lymphedema_hypoparathyroidism.htm. Retrieved 2012-08-24.
2. ↑ Dahlberg (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

* Dahlberg Borer Newcomer syndrome at Orphanet

## External links

Classification|

* ICD-10: Q87.8
* OMIM: 247410
* MeSH: C535769

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External resources|

* Orphanet: 1563

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