Hemoglobinopathy Toms River
Synonyms: Transient neonatal cyanosis and anemia due to Toms River Hemoglobin
Hemoglobinopathy Toms River is a rare genetic hemoglobinopathy disorder due to a defect in the gamma subunit of the fetal hemoglobin characterized by neonatal cyanosis low hemoglobin oxygen saturation levels without arterial hypoxemia moderate anemia and reticulocytosis not associated with heart or lung disease. Symptoms progressively subside within the first months of life.
Data from Orphanet are used to provide information on a disease's name, synonym(s), and overview.
Reference: Access aggregated data from Orphanet at Orphadata.
Orphadata: Free access data from Orphanet. © INSERM 1999. Available on http://www.orphadata.org. Data version April 2024
Newly diagnosed with
Hemoglobinopathy Toms River?
Our RARE Concierge Services Guides are available to assist you by providing information, resources and connections as you navigate your rare disease journey.
Clinical Trials
For a list of clinical trials in this disease area, please click here.