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Libyan Journal of Medicine Volume 8, 2013 - Issue 1

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Frequency and spectrum of Wolcott–Rallison syndrome in Saudi Arabia: a systematic review

Abdelhadi M. HabebEndocrine and Diabetes Unit, Maternity and Children Hospital, Al-Madinah, Saudi ArabiaCorrespondence[email protected]

Article: 21137 | Received 16 Apr 2013, Accepted 16 May 2013, Published online: 10 Jun 2013

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https://doi.org/10.3402/ljm.v8i0.21137

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Millad Ghawil, Fathia Abdulrahman, Ibtisam Hadeed, Milad Doggah, Salem Zarroug & Abdelhadi Habeb. (2022) Further evidence supporting the role of DUT gene in diabetes with bone marrow failure syndrome . American Journal of Medical Genetics Part A 188:8, pages 2406-2412.
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Mohsina Noor Ibrahim, Taj Muhammad Laghari, Miara Riaz, Zubair Khoso, Yasir Naqi Khan, Mehar Yasir, Misbah Iqbal Hanif, Sarah E. Flanagan, Elisa De Franco & Jamal Raza. (2021) Monogenic diabetes in Pakistani infants and children: challenges in a resource poor country. Journal of Pediatric Endocrinology and Metabolism 34:9, pages 1095-1103.
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Andrea Sümegi, Zoltán Hendrik, Tamás Gáll, Enikő Felszeghy, Katalin Szakszon, Péter Antal-Szalmás, Lívia Beke, Ágnes Papp, Gábor Méhes, József Balla & György Balla. (2020) A novel splice site indel alteration in the EIF2AK3 gene is responsible for the first cases of Wolcott-Rallison syndrome in Hungary. BMC Medical Genetics 21:1.
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Johan Nordström, Markus Lundgren, Carl Jorns, Björn Fischler, Henrik Arnell, Rafal Dlugosz, John Sandberg, Lars Wennberg & Greg Nowak. (2020) First European Case of Simultaneous Liver and Pancreas Transplantation as Treatment of Wolcott-Rallison Syndrome in a Small Child. Transplantation 104:3, pages 522-525.
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Tarah H. Fatani. (2019) EIF2AK3 novel mutation in a child with early-onset diabetes mellitus, a case report. BMC Pediatrics 19:1.
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Markus Lundgren, Elisa De Franco, Henrik Arnell & Björn Fischler. (2019) Practical management in Wolcott‐Rallison syndrome with associated hypothyroidism, neutropenia, and recurrent liver failure: A case report. Clinical Case Reports 7:6, pages 1133-1138.
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Farzaneh Abbasi, Maryam Habibi, Samaneh Enayati, Fatemeh Bitarafan, Maryam Razzaghy-Azar, Aria Sotodeh, Sima Parvizi Omran, Reza Maroofian & Mahsa M. Amoli. (2018) A Genotype-First Approach for Clinical and Genetic Evaluation of Wolcott-Rallison Syndrome in a Large Cohort of Iranian Children With Neonatal Diabetes. Canadian Journal of Diabetes 42:3, pages 272-275.
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Asma Deeb, Abdelhadi Habeb, Walid Kaplan, Salima Attia, Suha Hadi, Amani Osman, Jamal Al-Jubeh, Sarah Flanagan, Elisa DeFranco & Sian Ellard. (2016) Genetic characteristics, clinical spectrum, and incidence of neonatal diabetes in the Emirate of AbuDhabi, United Arab Emirates. American Journal of Medical Genetics Part A 170:3, pages 602-609.
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Sophie Collardeau-Frachon, Alexandre Vasiljevic, Anne Jouvet, Raymonde Bouvier, Valérie Senée & Marc Nicolino. (2015) Microscopic and ultrastructural features in Wolcott-Rallison syndrome, a permanent neonatal diabetes mellitus: about two autopsy cases. Pediatric Diabetes 16:7, pages 510-520.
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Abdelhadi M. Habeb, Asma Deeb, Matthew Johnson, Mohammed Abdullah, Majidah Abdulrasoul, Hussain Al-Awneh, Mohammed S.F. Al-Maghamsi, Fathiya Al-Murshedi, Ramlah Al-Saif, Siham Al-Sinani, Dina Ramadan, Hala Tfayli, Sarah E. Flanagan & Sian Ellard. (2015) Liver Disease and Other Comorbidities in Wolcott-Rallison Syndrome: Different Phenotype and Variable Associations in a Large Cohort. Hormone Research in Paediatrics 83:3, pages 190-197.
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Frequency and spectrum of Wolcott–Rallison syndrome in Saudi Arabia: a systematic review

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Frequency and spectrum of Wolcott–Rallison syndrome in Saudi Arabia: a systematic review

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