MECP2 Gene-Related Severe Neonatal Encephalopathy: A Rare Case in a Female Neonate
Neonatal encephalopathy is a common morbidity witnessed by neonatologists globally. Though hypoxic ischemic encephalopathy (HIE) is the most common cause of neonatal encephalopathy, the absence of a specific history of hypoxia-ischemia necessitates knowledge about other diseases causing encephalopathy among neonates. These include a plethora of central nervous system, neuromuscular, vascular, metabolic, and genetic disorders. We describe a rare case of neonatal encephalopathy caused by a Methyl CpG binding protein 2 (MECP2) gene mutation in a female neonate. MECP2 mutations mostly lead to classical or variant Rett syndrome in females with a later presentation, while neonatal encephalopathy is almost exclusively reported in males. The case highlights the need for genetic testing for non-HIE causes of neonatal encephalopathy to attain the correct diagnosis.
Authors
- Risha Devi (ORCID: https://orcid.org/0009-0004-9453-9572)
- Mayank Priyadarshi
- Poonam Singh
- Deeksha Gupta
- Sriparna Basu
- Pavan K RC
- Suman Chaurasia
Institutions
- Seema Dental College and Hospital (IN)
- All India Institute of Medical Sciences Rishikesh (IN)
Publication Details
- Journal
- Cureus
- Published
- 2026-01-15
- DOI
- https://doi.org/10.7759/cureus.101620
- Primary Topic
- Genetics and Neurodevelopmental Disorders
- Type
- article
- Field-Weighted Citation Impact
- 0.00