Lipoyltransferase 1 Gene Defect Resulting in Fatal Lactic Acidosis in Two Siblings
A term male neonate developed severe intractable lactic acidosis on day of life 1 and died the same day at our institution. The family previously lost another term, female newborn on day of life 1 from suspected sepsis at an outside hospital. After performing an autopsy on the neonate who died at ou...
Main Authors: | Véronique Taché, Liga Bivina, Sophie White, Jeffrey Gregg, Joshua Deignan, Simeon A. Boyadjievd, Francis R. Poulain |
---|---|
Format: | Article |
Language: | English |
Published: |
Hindawi Limited
2016-01-01
|
Series: | Case Reports in Obstetrics and Gynecology |
Online Access: | http://dx.doi.org/10.1155/2016/6520148 |
Similar Items
-
Functional Assessment of Lipoyltransferase-1 Deficiency in Cells, Mice, and Humans
by: Min Ni, et al.
Published: (2019-04-01) -
091 SEVERE METFORMIN ASSOCIATED LACTIC ACIDOSIS: A NOT SO RARE AND POTENTIALLY FATAL COMPLICATION
by: K.H. Lai, et al.
Published: (2017-08-01) -
Viekira Pak Induced Fatal Lactic Acidosis: A Case Report of an Unusual Side Effect
by: Molham Abdulsamad, et al.
Published: (2016-01-01) -
Etiology of lactic acidosis in malaria.
by: Hendrik Possemiers, et al.
Published: (2021-01-01) -
Lactic acidosis associated to metformin
by: María Juliana Zavala Portugal, et al.
Published: (2017-06-01)