hrp0082p2-d2-297 | Bone (1) | ESPE2014
Raimann Adalbert
, Alexandra Ertl Diana
, Riedl Stefan
, Schlegel Werner
, Haeusler Gabriele
Background: Progressive osseous heteroplasia (POH) is a rare condition characterized by extensive heterotopic ossification (HO) of connective tissues. Associations of HO and Albright hereditary dystrophy (AHO) lead to the identification of GNAS mutations to be causative for ectopic none formations. The highly imprinted GNAS locus is known to cause a broad spectrum of pathologic conditions, including pseudohypoparathyrodism (PHP), pseudoPHP AHO. While PHP is caused by maternal ...