Isovaleric Acidemia as a Rare Cause for Bad Obstetric History
Isovaleric acidemia is an inborn error of metabolism, inherited as an autosomal recessive disorder, caused by deficiency of isovalerylCoenzyme A (CoA) dehydrogenase, leading to elevated plasma isovaleric acid and urine isovalerylglycine levels. Isovaleric acidemia is an unusual disorder with an inc...
Saved in:
Main Authors: | Sailatha Ramanujam, Shery Angel, Anuradha Coimbatore Ramachandran, Anu Bhargavi Basker |
---|---|
Format: | article |
Language: | EN |
Published: |
JCDR Research and Publications Private Limited
2021
|
Subjects: | |
Online Access: | https://doaj.org/article/cfbab62db94d41d78f76d11264ed1ff0 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Inherited metabolic diseases: aminoacidopathies, organic acidemia, defects of mitochondrial β-oxidation. A brief overview
by: O. V. Bugun, et al.
Published: (2021) -
Tamiz de los errores innatos del metabolismo por espectrometría de masas en tándem: principales biomarcadores
by: Campos H,Derbis
Published: (2011) -
Positive improvement in palatability of metabolic formula with the use of miraculin protein in patients with inborn errors of metabolism and healthy adults
by: López,Lizbeth, et al.
Published: (2020) -
Reconciling the Uniquely Embodied Grief of Perinatal Death: A Narrative Approach
by: Tamarin Norwood, et al.
Published: (2021) -
Diagnosis and Management of Inborn Errors of Metabolism in Adult Patients in the Emergency Department
by: Isabel Solares, et al.
Published: (2021)