Sickle Cell Disease

2025-04-02 16:23:25 - Admin Name

SubsetsSickle Cell Trait:

HbSA (± 10% population) Heterozygocity for HbS (sickle cell trait): usually asymptomatic, lower parasitemia, higher Hb

Sickle Cell Disease:

HbSS (<1% population) Homozygocity for HbS or HbS+C/β: change in Hb structure, sickling if deoxygenated

Making the Diagnosis

Important points in historyImportant points on examinationInvestigationsTreatment (general)AnaemiaPainful & vaso-occlusive crisesAnalgesia - Regular Medicine, not PRN

(Pain Management )

Infections and Fever (functional asplenia from 6 months)OthersSpecific Management
Discharge & Long-term follow-up

Send to sickle cell clinic.

In QECH it takes place Tuesdays at 13:30 in Paediatrics Under 5 for:

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