Difference between revisions of "Birt–Hogg–Dubé syndrome"

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**[[Renal hybrid oncocytic/chromophobe tumour]].<ref name=pmid23740406>{{Cite journal  | last1 = Hes | first1 = O. | last2 = Petersson | first2 = F. | last3 = Kuroda | first3 = N. | last4 = Hora | first4 = M. | last5 = Michal | first5 = M. | title = Renal hybrid oncocytic/chromophobe tumors - a review. | journal = Histol Histopathol | volume = 28 | issue = 10 | pages = 1257-64 | month = Oct | year = 2013 | doi =  | PMID = 23740406 }}</ref>
**[[Renal hybrid oncocytic/chromophobe tumour]].<ref name=pmid23740406>{{Cite journal  | last1 = Hes | first1 = O. | last2 = Petersson | first2 = F. | last3 = Kuroda | first3 = N. | last4 = Hora | first4 = M. | last5 = Michal | first5 = M. | title = Renal hybrid oncocytic/chromophobe tumors - a review. | journal = Histol Histopathol | volume = 28 | issue = 10 | pages = 1257-64 | month = Oct | year = 2013 | doi =  | PMID = 23740406 }}</ref>
* Variable penetrance (autosomal dominant).
* Variable penetrance (autosomal dominant).
Note:
*May be seen with a mix of oncocytic renal tumours - known as ''[[renal oncocytosis]]''.


==See also==
==See also==

Revision as of 04:14, 4 December 2015

Birt–Hogg–Dubé syndrome, also Hornstein-Birt-Hogg-Dubé syndrome,[1] is constellation of findings due to a FLCN (folliculin) gene mutation.[2] It is abbreviated BHD syndrome.

Features

BHD syndrome is characterized by:[3]

Note:

See also

References

  1. Happle, R. (Jun 2012). "Hornstein-Birt-Hogg-Dubé syndrome: a renaming and reconsideration.". Am J Med Genet A 158A (6): 1247-51. doi:10.1002/ajmg.a.35330. PMID 22581760.
  2. Online 'Mendelian Inheritance in Man' (OMIM) 135150
  3. Humphrey, Peter A; Dehner, Louis P; Pfeifer, John D (2008). The Washington Manual of Surgical Pathology (1st ed.). Lippincott Williams & Wilkins. pp. 290. ISBN 978-0781765275.
  4. Hes, O.; Petersson, F.; Kuroda, N.; Hora, M.; Michal, M. (Oct 2013). "Renal hybrid oncocytic/chromophobe tumors - a review.". Histol Histopathol 28 (10): 1257-64. PMID 23740406.