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Causes of Global Developmental Delay in Children Welfare Teaching Hospital-Baghdad | ||
| Iraqi Postgraduate Medical Journal | ||
| Article 1, Volume 12, Issue 3, 2013, Pages 383-389 PDF (0 K) | ||
| Authors | ||
| Shaima Hussein Alwan; Mohammad F. Ibraheem; Mahjoob Al-Naddawi | ||
| Abstract | ||
| ABSTRACT: BACKGROUND: There are wide ranges of causes behind global developmental delay in Iraqi children but most of these causes were not diagnosed as a result of unavailable diagnostic tools. OBJECTIVE: To study the etiology of global developmental delay in Children Welfare Teaching Hospital / Baghdad. PATIENTS AND METHODS: A descriptive study was done on 75 patients, their age range from 8 months to 5.5 years with global developmental delay, who consult Children Welfare Teaching Hospital/Baghdad, from 1 of May 2010 to 1 st of October 2010. A full history, thorough physical examination, and developmental assessment according to Denver Developmental Scale II were done to all cases. A group of selected investigations including neuroimaging (CT & MRI), EMG, EEG, visual and hearing assessment, screen for metabolic diseases, and thyroid function test were done as needed for the diagnosis. RESULTS: A total of 75(preschool) patients with age range from 8 months to 5.5 years were studied; 45(60%) of them were males and 30(40%) were females,9(12%) were preterm, 26(34.6%) were born with LBW, 3(4%) of patients acquired the infection with TORCH from their mothers [2(2.7%)CMV, 1(1.3%)toxoplasmosis], 8(10.7%) had their mothers complained from chronic diseases (hypertension and diabetes mellitus ), 11(14.7%) suffered birth asphyxia, 2(2.7%) with high bilirubin level exceeding 20mg/dl, 2(2.7%) patients suffered RDS and 1(1.3%) suffered sepsis diagnosed by blood culture during neonatal period .Family history of developmental delay was reported in 11(14.7%) and consanguinity was reported in 46(61.3%) of cases, in 33(43.9%) no cause could be identified, CNS infections 9(12%), Down syndrome 7(9.3%), hypothyroidism 2(2.7%), intracranial hemorrhage 2(2.7%), infantile spasm 2(2.7%), phenylketonuria 2(2.7%), Myotonia Dystrophica 1(1.3%), and Seckel syndrome 1(1.3%). CONCLUSION: Global developmental delay in pediatric practice has wide etiology. The majority of cases were not diagnosed because of deficient diagnostic tools like cytogenetic analysis. High percent of perinatal etiology raises the importance of good maternal and neonatal care. Under diagnosis of inborn error of metabolism due to lack of routine screening in neonatal period, aggravated the problem | ||
| Keywords | ||
| global developmental | ||
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