Helen Michelakakis
Biographic Data
| ID | 7610373 |
|---|---|
| NAME | Helen Michelakakis |
| GIVEN NAMES | Helen |
| FAMILY NAME | Michelakakis |
| SIGNATURE | MICHELAKAKIS H |
| AFFILIATIONS | Institute of Child Health |
| ORCID | 0000-0002-1858-891X |
| VERIFIED | Yes |
| TOTAL WORKS | 1 |
| TOTAL CITATIONS | 0 |
| WORKS AS AUTHOR | 1 |
| WORKS AS EDITOR | 0 |
| FIRST PUBLICATION YEAR | 2021 |
| LATEST PUBLICATION YEAR | 2021 |
| H-INDEX | 0 |
Hemolytic Uremic Syndrome Due to Methylmalonic Acidemia and Homocystinuria in an Infant
Methylmalonic acidemia and homocystinuria cobalamin C (cblC) type is the most common inborn error of the intracellular cobalamin metabolism, associated with multisystem involvement and high mortality rates, especially in the early-onset form of the disease. Hemolytic uremic syndrome (HUS) is a rare manifestation and needs to be distinguished from other causes of renal thrombotic microangiopathy. We describe a case of a 3-month-old infant, with fa…
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Hemolytic Uremic Syndrome Due to Methylmalonic Acidemia and Homocystinuria in an Infant
Methylmalonic acidemia and homocystinuria cobalamin C (cblC) type is the most common inborn error of the intracellular cobalamin metabolism, associated with multisystem involvement and high mortality rates, especially in the early-onset form of the disease. Hemolytic uremic syndrome (HUS) is a rare manifestation and needs to be distinguished from other causes of renal thrombotic microangiopathy. We describe a case of a 3-month-old infant, with fa…
cobalamin (1 work) · Failure to thrive (1 work) · Folate and B Vitamins Research (1 work) · Gastroenterology (1 work) · Genetics (1 work) · Homocystinuria (1 work) · Hypotonia (1 work) · Internal Medicine (1 work) · Medicine (1 work) · Metabolism and Genetic Disorders (1 work)