Autosomal dominant transmission of transient neonatal lactic acidosis: a case report
Abstract Background Lactic acidosis is a common finding in neonates, in whom mitochondrial dysfunction is often secondary to tissue hypoperfusion, respiratory failure, and/or sepsis. Primary (non-physiological) lactic acidosis is comparatively rare, and suggests the presence of an inborn error of mi...
Main Authors: | Emily B. Mardian, Matthew A. Lines, Care4Rare Consortium, Gregory P. Moore |
---|---|
Format: | Article |
Language: | English |
Published: |
BMC
2020-04-01
|
Series: | BMC Pediatrics |
Subjects: | |
Online Access: | http://link.springer.com/article/10.1186/s12887-020-02085-x |
Similar Items
-
Metformin-associated lactic acidosis: it really happens!
by: Faisal Hasan, et al.
Published: (2017-01-01) -
Lactic acidosis, hyperlactatemia and sepsis
by: Andrea Montagnani, et al.
Published: (2016-12-01) -
Acidosis láctica
by: Caridad Soler Morejón
Published: (2000-06-01) -
Severe acute lactic acidosis and hypoglycemia due to isolate tramadol poisoning
by: Patricia Granauro, et al.
Published: (2016-06-01) -
Alkali Therapy in Lactic Acidosis
by: Zeid J. Khitan, et al.
Published: (2015-01-01)