Abstract
A case of hereditary spherocytosis in a newborn Negro male is presented. The methods of establishing thediagnosis of hereditary spherocytosis in the neonatal period are discussed. Hereditary spherocytosis is due, in all probability, to multiple genetic factors, and these may be operating in utero. The question of splenectomy in infants with hereditary spherocytosis is discussed. A case of hereditary spherocytosis in a newborn Negro male is presented. The methods of establishing thediagnosis of hereditary spherocytosis in the neonatal period are discussed. Hereditary spherocytosis is due, in all probability, to multiple genetic factors, and these may be operating in utero. The question of splenectomy in infants with hereditary spherocytosis is discussed.
Sign-in/Register to access full text options 
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callDisclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
