A 3-Month-Old Boy With Progressive Weakness

Brain Pathol. 2018 Sep;28(5):773-774. doi: 10.1111/bpa.12651.

Authors

Soo Yeon Kim¹, Jung Min Ko², Sun Ah Choi¹, Anna Cho³, Jin Sook Lee⁴, Byung Chan Lim¹, Ki Joong Kim¹, Jong-Hee Chae¹

Affiliations

¹ Department of Pediatrics, Pediatric Clinical Neuroscience Center, Seoul National University Children's Hospital, Seoul, Korea.
² Department of Genetics, Seoul National University College of Medicine, Seoul, Korea.
³ Department of Pediatrics, Ewha Woman's University School of Medicine, Seoul, Korea.
⁴ Department of Pediatrics, Gachon University Gil Medical Center, Incheon, Korea.

No abstract available

Publication types

Case Reports

MeSH terms

Child, Preschool
Diagnosis, Differential
Electron-Transferring Flavoproteins / deficiency
Electron-Transferring Flavoproteins / genetics
Humans
Iron-Sulfur Proteins / deficiency
Iron-Sulfur Proteins / genetics
Male
Multiple Acyl Coenzyme A Dehydrogenase Deficiency / diagnosis*
Multiple Acyl Coenzyme A Dehydrogenase Deficiency / genetics
Multiple Acyl Coenzyme A Dehydrogenase Deficiency / pathology
Muscle Weakness / diagnosis*
Muscle Weakness / genetics
Muscle Weakness / pathology
Muscle, Skeletal / pathology
Oxidoreductases Acting on CH-NH Group Donors / deficiency
Oxidoreductases Acting on CH-NH Group Donors / genetics

Substances

Electron-Transferring Flavoproteins
Iron-Sulfur Proteins
Oxidoreductases Acting on CH-NH Group Donors
electron-transferring-flavoprotein dehydrogenase