2022
DOI: 10.18502/acta.v60i9.11102
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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

Abstract: 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. Special features included microcephaly, microstomia, full lips, micrognathia, narrow convex, and high nasal bridge nose. Also, it may be accompanied by feeding problems, skeletal disorders, urogenital or respiratory… Show more

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“…Various factors may be associated with childhood obesity including nutrition in early life, excessive gestational weight gain,[ 2 ] maternal smoking during pregnancy, parent feeding practices, duration of breastfeeding, body mass index (BMI), father's weight, birth order, age, birth weight, and rapid weight gain (RWG). [ 3 4 ]…”
Section: Introductionmentioning
confidence: 99%
“…Various factors may be associated with childhood obesity including nutrition in early life, excessive gestational weight gain,[ 2 ] maternal smoking during pregnancy, parent feeding practices, duration of breastfeeding, body mass index (BMI), father's weight, birth order, age, birth weight, and rapid weight gain (RWG). [ 3 4 ]…”
Section: Introductionmentioning
confidence: 99%