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The Journal of Maternal-Fetal & Neonatal Medicine Volume 29, 2016 - Issue 12
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Original Article

A review of Meckel–Gruber syndrome – incidence and outcome in the state of Qatar

Mariam Al-BelushiFetal-Maternal Medicine Unit, Women’s Hospital Hamad Medical Corporation, Doha, Qatar, Correspondence[email protected]
,
Abdullah Al IbrahimFetal-Maternal Medicine Unit, Women’s Hospital Hamad Medical Corporation, Doha, Qatar,
,
Mayada AhmedFetal-Maternal Medicine Unit, Women’s Hospital Hamad Medical Corporation, Doha, Qatar,
,
Badredeen AhmedFetal-Maternal Medicine Unit, Women’s Hospital Hamad Medical Corporation, Doha, Qatar, ;Fetal Medicine Center, Doha, Qatar, and
,
Najat KhenyabFetal-Maternal Medicine Unit, Women’s Hospital Hamad Medical Corporation, Doha, Qatar,
&
Justin C KonjeFetal-Maternal Medicine Unit, Women’s Hospital Hamad Medical Corporation, Doha, Qatar, ;Department of Obstetrics and Gynecology, Sidra Medical and Research Centre, Doha, Qatar
Pages 2013-2016 | Received 09 May 2015, Accepted 09 Jul 2015, Published online: 26 Aug 2015

Citations (5)

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Read on this site (1)

Kiran Pandurang Sawardekar. (2016) Meckel–Gruber syndrome: prevalence from a hospital-based study in Oman. The Journal of Maternal-Fetal & Neonatal Medicine 29:22, pages 3696-3698.
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Articles from other publishers (4)

Mohamad Alsamal, Osama A. Zitoun, Ebtsam Abdulaziz Abdulghani & Idris Sula. (2023) Meckel–Gruber syndrome together with Dandy–Walker malformation: an atypical case report of a 2nd recurrence in a consanguine marriage. Child's Nervous System.
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Montse Pauta, Raigam Jafet Martinez-Portilla & Antoni Borrell. (2021) Prenatal Exome Sequencing in Recurrent Fetal Structural Anomalies: Systematic Review and Meta-Analysis. Journal of Clinical Medicine 10:20, pages 4739.
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Konstantin Ridnõi, Marek Šois, Eve Vaidla, Sander Pajusalu, Larissa Kelder, Tiia Reimand & Katrin Õunap. (2019) A prenatally diagnosed case of Meckel–Gruber syndrome with novel compound heterozygous pathogenic variants in the TXNDC15 gene . Molecular Genetics & Genomic Medicine 7:5, pages e614.
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Zuzana Cierna, Pavol Janega, Frantisek Grochal, Vladimir Ferianec, Tatiana Braxatorisova, Lucia Strieskova, Jana Malova, Petra Jungova & Tomas Szemes. (2017) The First Reported Case of Meckel–Gruber Syndrome Associated With Abnormal Karyotype Mosaic Trisomy 17. Pediatric and Developmental Pathology 20:5, pages 449-454.
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