Riga Fede Disease with Glutaric Aciduria Type 1

Indian J Pediatr. 2020 Jun;87(6):484-485. doi: 10.1007/s12098-019-03125-w. Epub 2019 Dec 6.

Authors

Palanisamy Sivamurukan¹, Venkatesh Chandrasekaran², Niranjan Biswal²

Affiliations

¹ Department of Pediatrics, Jawaharlal Institute of Postgraduate Medical Education and Research (JIPMER), Pondicherry, 605006, India. sivamurukan@gmail.com.
² Department of Pediatrics, Jawaharlal Institute of Postgraduate Medical Education and Research (JIPMER), Pondicherry, 605006, India.

PMID: 31811503
DOI: 10.1007/s12098-019-03125-w

No abstract available

Publication types

Case Reports

MeSH terms

Amino Acid Metabolism, Inborn Errors* / diagnosis
Brain Diseases, Metabolic* / diagnosis
Brain Diseases, Metabolic* / etiology
Female
Glutaryl-CoA Dehydrogenase / deficiency
Humans
Infant
Oral Ulcer*

Substances

Glutaryl-CoA Dehydrogenase

Supplementary concepts

Glutaric Acidemia I