An 11-Year-Old Girl With Rare Diagnosis of Meier-Gorlin Syndrome Accompanied by Neonatal Seizure, Mental Retardation, and Attention Deficit Hyperactivity Disorder: A Case Report and Review of Literature

An 11-Year-Old Girl With Rare Diagnosis of Meier-Gorlin Syndrome Accompanied by Neonatal Seizure, Mental Retardation, and Attention Deficit Hyperactivity Disorder: A Case Report and Review of Literature

Meier-Gorlin syndrome (MGS) is a rare autosomal recessive disorder with homozygous or heterozygous mutations in one of the five following genes (ORC1, ORC4, ORC6, CDT1, and CDC6). This syndrome is characterized by the triad of short stature (pre/postnatal), microtia, and patella hypoplasia/aplasia....

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Bibliographic Details
Main Authors: Shahin Koomanaee, Setila Dalili, Seyyedeh Azade Hoseini Nouri, Seyedeh Zohreh Jalali, Manijeh Tabrizi, Ghazaleh Aldaghi, Afagh Hassanzadeh Rad
Format: Article
Language:English
Published: Tehran University of Medical Sciences 2022-11-01
Series:Acta Medica Iranica
Subjects:
Meier-Gorlin syndrome
Seizures
Intellectual disability
Neonatal seizure
Attention deficit disorder with hyperactivity
Online Access:https://acta.tums.ac.ir/index.php/acta/article/view/10123

Internet

https://acta.tums.ac.ir/index.php/acta/article/view/10123

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