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Keywords: Mowat-Wilson syndrome
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Journal Articles
Subject Area:
Karger e-Journal Backfile Collection 2023
, Endocrinology
, Further Areas
, Genetics
, Women's and Children's Health
Journal:
Molecular Syndromology
Mol Syndromol (2023) 14 (3): 258–266.
Published Online: 06 June 2023
...Naz Güleray Lafcı; Beren Karaosmanoglu; Ekim Z. Taskiran; Pelin Ozlem Simsek-Kiper; Gülen Eda Utine Introduction: Mowat-Wilson syndrome (MWS) is an autosomal-dominant complex developmental disorder characterized by distinctive facial appearance, intellectual disability, epilepsy, and various...
Journal Articles
Subject Area:
Topic Article Package: Moksha
, Endocrinology
, Further Areas
, Genetics
, Women's and Children's Health
Khaled Refaat, Nivine Helmy, Mohamed Elawady, Mona El Ruby, Alaa Kamel, Mona Mekkawy, Engy Ashaat, Ola Eid, Amal Mohamed, Mervat Rady
Journal:
Molecular Syndromology
Mol Syndromol (2021) 12 (2): 87–95.
Published Online: 01 March 2021
...Khaled Refaat; Nivine Helmy; Mohamed Elawady; Mona El Ruby; Alaa Kamel; Mona Mekkawy; Engy Ashaat; Ola Eid; Amal Mohamed; Mervat Rady Mowat-Wilson syndrome (MWS) is a rare autosomal dominant syndrome characterized by dysmorphic features, mental retardation, and congenital heart disease (CHD). MWS...
Journal Articles
Subject Area:
Topic Article Package: Moksha
, Endocrinology
, Further Areas
, Genetics
, Women's and Children's Health
Durdugul Ayyildiz Emecen, Esra Isik, Gulen E. Utine, Pelin O. Simsek-Kiper, Tahir Atik, Ferda Ozkinay
Journal:
Molecular Syndromology
Mol Syndromol (2020) 11 (5-6): 296–301.
Published Online: 20 November 2020
...Durdugul Ayyildiz Emecen; Esra Isik; Gulen E. Utine; Pelin O. Simsek-Kiper; Tahir Atik; Ferda Ozkinay Mowat-Wilson syndrome (MWS) is a rare autosomal dominant syndrome characterized by distinctive facial features, congenital heart defects, Hirschsprung disease, genitourinary anomalies, various...
Journal Articles
Adrianne L. Baxter, Jay L. Vivian, R. Tanner Hagelstrom, Waheeda Hossain, Wendy L. Golden, E. Robert Wassman, Rena J. Vanzo, Merlin G. Butler
Journal:
Molecular Syndromology
Mol Syndromol (2017) 8 (4): 211–218.
Published Online: 03 May 2017
...Adrianne L. Baxter; Jay L. Vivian; R. Tanner Hagelstrom; Waheeda Hossain; Wendy L. Golden; E. Robert Wassman; Rena J. Vanzo; Merlin G. Butler Mowat-Wilson syndrome is a rare genetic condition characterized by intellectual disability, structural anomalies, and dysmorphic features. It is caused...
