Review
Copyright ©The Author(s) 2020.
World J Gastroenterol. Nov 28, 2020; 26(44): 6909-6922
Published online Nov 28, 2020. doi: 10.3748/wjg.v26.i44.6909
Table 1 Gene/chromosome mutations related to pituitary stalk interruption syndrome
Ref.
Gene/chromosome
Liu et al[39], 2020ROBO1
Wang et al[40], 2020NBPF9
Bashamboo et al[29], 2016CDON
Guo et al[35], 2017NCOR2, NKD2, ZIC2, MAML3
Bashamboo et al[32], 2017ROBO1
Zwaveling-Soonawala et al[33], 2018DCHS1, ROBO2, CCDC88C, KIF14, KAT6A, GLI2, PROK2, NR0B1, DCHR7, CCD2DA
Yang et al[26], 2013HESX1, LHX4, SOX3
Tatsi et al[30], 2013TGIF, SHH
Wang et al[41], 2019MUC4, NBPF10
El Chehadeh-Djebbar et al[38], 201117q21.31 microdeletion
Reynaud et al[27], 2012PROKR2, HESX1
Fang et al[42], 2020PTCH1, PTCH2, GLI2, TCTN1, ATR, GLI1, CDON, CREBBP, KIF7, LHX4, HHAT, STK36, MAPK3, SMO, PRKAR2A, PRKAR2B, EGR4, SPG11, AHI1, CHD7, CAD, CEP152, CEP290, DHCR24, DMXL2, FREM1, GPSM2, ISPD, NIN, ROBO2, SIX4, SLIT2, WDR11, ASPM, CENPJ, CEP41, DIS3L2, DISC1, DSC2, GH1, GNAS, LRP2, MARCKS, MYH10, NPHP1, NSD1, OTUD4, PCSK1, POMGNT1,PSEN1, RNF111, STIL, TACR3, TBC1D32, VIPR2, WNT5A, ZEB2, ZNF423
Reynaud et al[43], 2006LHX4
Dateki et al[44], 2019ROBO1
McCormack et al[34], 2017PROKR2, WDR11
Demiral et al[45], 2020GLI2
Reynaud et al[4], 2011HESX1, LHX4
Diaczok et al[23], 2008OTX2
Han et al[28], 2016PROKR2
Coutinho et al[46], 2019HESX1
Vetro et al[37], 2014Chromosome 2p25 and 2q37
Woods et al[24], 2005SOX3
Castinetti et al[25], 2008LHX4
Karaca et al[31], 2015GPR161
Carvalhom et al[22], 2003HESX1
Fernandez-Rodriguez et al[11], 2011PROP1
Yang et al[36], 2019De novo 18p deletion