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Sickle Cell Disorder: A Family Study With Eight Homozygous and Two Heterozygous Children | Synapse
March 3, 2026
Sickle Cell Disorder: A Family Study With Eight Homozygous and Two Heterozygous Children
SK
Sudam L. Kate
GY
Gunvant H. Yeola
PD
Prashant N. Dalvi
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Key Points
Sickle cell disorder significantly impacts genetic inheritance patterns in children.
The family study includes eight homozygous and two heterozygous children, highlighting diverse genotypes.
Genetic inheritance was analyzed among family members to assess the risk of sickle cell disorder.
Findings underscore the need for genetic counseling in families affected by sickle cell disease.
Abstract
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Kate et al. (Fri,) studied this question.
synapsesocial.com/papers/69a765a9badf0bb9e87d9f49