Sook Kyung Yum
Biographic Data
| ID | 8266747 |
|---|---|
| NAME | Sook Kyung Yum |
| GIVEN NAMES | Sook Kyung |
| FAMILY NAME | Yum |
| SIGNATURE | YUM S K |
| AFFILIATIONS | The Catholic University of Korea Seoul St. Mary's Hospital |
| ORCID | 0000-0001-8589-3159 |
| VERIFIED | Yes |
| TOTAL WORKS | 1 |
| TOTAL CITATIONS | 0 |
| AUTHOR COUNT | 1 |
| EDITOR COUNT | 0 |
| FIRST PUBLICATION YEAR | 2023 |
| LATEST PUBLICATION YEAR | 2023 |
| H-INDEX | 0 |
Mimicking Hypoxic-Ischemic Encephalopathy in a Newborn with 21q Deletion Originating from Ring Chromosome 21
Partial deletion of the long arm (q) in chromosome 21 is an extremely rare condition with various phenotypes, including microcephaly, neurodevelopmental delay, dysmorphic features, and epileptic seizures. Neonatal hypoxic-ischemic encephalopathy (HIE) is an encephalopathy associated with a hypoxic-ischemic event in the brain where seizures usually occur in the earliest days of life. Neonatal encephalopathy is a distinct entity resulting from meta…
No prominent works on this page.
Mimicking Hypoxic-Ischemic Encephalopathy in a Newborn with 21q Deletion Originating from Ring Chromosome 21
Partial deletion of the long arm (q) in chromosome 21 is an extremely rare condition with various phenotypes, including microcephaly, neurodevelopmental delay, dysmorphic features, and epileptic seizures. Neonatal hypoxic-ischemic encephalopathy (HIE) is an encephalopathy associated with a hypoxic-ischemic event in the brain where seizures usually occur in the earliest days of life. Neonatal encephalopathy is a distinct entity resulting from meta…
Abnormality (1 works) · Biology (1 works) · Encephalopathy (1 works) · Fetal and Pediatric Neurological Disorders (1 works) · Genetic counseling (1 works) · Genetic testing (1 works) · Genetics (1 works) · Hypotonia (1 works) · Hypoxic-Ischemic Encephalopathy (1 works) · Internal Medicine (1 works)