demographic and clinical findings in pediatric patients affected by organic acidemia

نویسندگان

reza najafi 1. pediatric endocrinology department, ilam university of medical sciences, ilam, iran

mahin hashemipour 2. pediatric endocrinology department, endocrine research center, isfahan

neda mostofizadeh 2. pediatric endocrinology department, endocrine research center, isfahan

mohammadreza ghazavi 3. pediatric neurology department, isfahan university of medical sciences, isfahan, iran

چکیده

how to cite this article: najafi r, hashemipour m, mostofizadeh n, ghazavi mr, nasiri j, shahsanai a, famori f, najafi f, moafi m. demographic and clinical findings in pediatric patients affected by organic acidemia. iran j child neurol. spring 2016; 10(2): 74-81. abstract objective metabolic disorders, which involve many different organs, can be ascribed to enzyme deficiency or dysfunction and manifest with a wide range of clinical symptoms. this study evaluated some of the demographic and clinical findings in pediatric patients affected by organic acidemia. materials & methods this cross-sectional study was part of a larger study conducted in patients with metabolic disorders during a period of 7 years from 2007 to 2014 in isfahan province, iran. our study covered a wide range of cases from newborn infants (one-week old) to adolescents (children up to the age of 17 years). this study evaluated patients’ demographic information, history of disease, developmental and educational status, clinical and general conditions. phone and in-person interviews were used to gather information. results out of 5100 patients screened in this study, 392 patients were affected by one of the different metabolic disorders and 167 individuals were diagnosed as organic acidemia. propionic acidemia/methyl malonic acidemia (pa/mma) was the most prevalent form of this metabolic disorder. the frequency of consanguinity was 84.7% in the group of patients. the mortality rate was 18.8% in patients with organic academia. conclusion each of the metabolic diseases, as a separate entity, is rare; 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عنوان ژورنال:
iranian journal of child neurology

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