hrp0089p1-p186 | Growth & Syndromes P1 | ESPE2018
Kawashima Sayaka
, Nakamura Akie
, Inoue Takanobu
, Matsubara Keiko
, Horikawa Reiko
, Wakui Keiko
, Takano Kyoko
, Fukushima Yoshimitsu
, Tatematsu Toshi
, Mizuno Seiji
, Tsubaki Junko
, Kure Shigeo
, Matsubara Yoichi
, Ogata Tsutomu
, Nagasaki Keisuke
, Fukami Maki
, Kagami Masayo
Context: Maternal uniparental disomy for chromosome 20 (UPD(20)mat) resulting in aberrant expression of imprinted transcripts at the GNAS locus is a poorly characterized condition. Only 10 non-mosaic cases have been studied clinically. These patients presented with pre- and post-natal growth failure and feeding difficulties. The phenotype of these cases overlapped with that of Silver-Russell syndrome (SRS) and small for gestational age-short stature (SGA-SS); however, the etio...