| Seow KM |
------>authors3_c=None ------>paper_class1=1 ------>Impact_Factor=None ------>paper_class3=2 ------>paper_class2=2 ------>vol=11 ------>confirm_bywho=tlc ------>insert_bywho=m001015 ------>Jurnal_Rank=None ------>authors4_c=None ------>comm_author= ------>patent_EDate=None ------>authors5_c=None ------>publish_day=None ------>paper_class2Letter=None ------>page2=81 ------>medlineContent= ------>unit=E0100 ------>insert_date=20040505 ------>iam=5 ------>update_date=None ------>author=??? ------>change_event=5 ------>ISSN=None ------>authors_c=None ------>score=-114 ------>journal_name=Adv Obstet Perinatol ------>paper_name=Early ultrasound diagnosis and management of cephalocele ------>confirm_date=20040507 ------>tch_id=092060 ------>pmid=12044856 ------>page1=73 ------>fullAbstract=We report of a case of Meckel Gruber Syndrome (MGS) in a woman, who suffered previously from a pregnancy with the same disorder. MGS, consisting of an occipital encephalocele, bilateral cystic kidneys and postaxial polydactyly, is a rare autosomal recessive disorder, with a recurrence risk of 25%. With the present technology, a targeted ultrasound in the late embryonic or early fetal stages of pregnancy has the potential to diagnose this syndrome. Clinical screening in further pregnancies is of utmost importance and the management of such cases is presented. ------>tmu_sno=None ------>sno=9009 ------>authors2=Cheng WC ------>authors3=Chang JZ ------>authors4=Tsai YL ------>authors5=Hwang JL ------>authors6= ------>authors6_c=None ------>authors=Seow KM ------>delete_flag=0 ------>SCI_JNo=None ------>authors2_c=None ------>publish_area=None ------>updateTitle=Meckel Gruber syndrome: a first trimester diagnosis of a recurrent case. ------>language=2 ------>check_flag=None ------>submit_date=None ------>country=None ------>no= ------>patent_SDate=None ------>update_bywho=None ------>publish_year=2000 ------>submit_flag=None ------>publish_month=None |