First report of congenital adrenal cysts and pheochromocytoma in a patient with mosaic genome-wide paternal uniparental disomy

Am J Med Genet A. 2016 Dec;170(12):3352-3355. doi: 10.1002/ajmg.a.37959. Epub 2016 Oct 12.

Authors

Mary White¹, George McGillivray², Sue M White^{2

3}, Margaret R Zacharin^{1

3}

Affiliations

¹ The Department of Endocrinology and Diabetes, The Royal Children's Hospital, Melbourne, Australia.
² Victorian Clinical Genetics Services, Murdoch Childrens Research Institute, Melbourne, Australia.
³ Department of Paediatrics, University of Melbourne, Melbourne, Australia.

PMID: 27734603
DOI: 10.1002/ajmg.a.37959

No abstract available

Publication types

Case Reports
Letter

MeSH terms

Adrenal Gland Diseases / complications
Adrenal Gland Diseases / diagnosis*
Cysts / complications
Cysts / diagnosis*
Female
Humans
Male
Mosaicism*
Pheochromocytoma / complications
Pheochromocytoma / diagnosis*
Uniparental Disomy*