Early infantile presentation of 3-methylcrotonyl CoA carboxylase deficiency: a case report

نویسندگان

چکیده

3-methylcrotonyl CoA carboxylase (3-MCC) deficiency is an inborn error of leucine amino acid metabolism. An isolated enzyme should be differentiated from biotin metabolism disorder which has all the four deficiencies. With advent tandem mass spectrometry (TMS), high number infants have been diagnosed with 3-MCC deficiency. Most neonates having appear normal, studies shown increased risk developmental and metabolic abnormalities. Universal newborn screening not routinely done in India. Many may missed at birth present symptoms later life. We reported a case half month old male infant seizures due to Very few data on available India hence this report.

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ژورنال

عنوان ژورنال: International Journal of Contemporary Pediatrics

سال: 2021

ISSN: ['2349-3283', '2349-3291']

DOI: https://doi.org/10.18203/2349-3291.ijcp20212060