Orthopaedic Complications of Sickle Cell Disease: A Review

Autor: Nwadinigwe, CU, Anyaehie, UE, Ogbu, DC, Muoghalu, O

Publikováno v: Nigerian Journal of Orthopaedics and Trauma; Vol 10, No 2 (2011); 81-88

Sickle cell disease (SCD) is a genetic disorder of mutant haemoglobin. It is inherited as an autosomal recessive disorder and is common in the West Africa subregion. Many of its orthopaedic complications require surgical intervention and many of its

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https://www.ajol.info/index.php/njotra/article/view/100929

Assessment of handgrip strength in healthy african subjects: Establishing age and gender stratified reference values.

Autor: I Essien UA; Department of Orthopaedics and Trauma, National Orthopaedic Hospital, Enugu, Nigeria., Amechi KU; Department of Accident and Emergency, University of Nigeria Teaching Hospital, Ituku-Ozalla, Nigeria., Madu KA; Department of Orthopaedics and Trauma, National Orthopaedic Hospital, Enugu, Nigeria., Ede O; Department of Orthopaedics and Trauma, National Orthopaedic Hospital, Enugu, Nigeria., Iyidobi EC; Department of Orthopaedics and Trauma, National Orthopaedic Hospital, Enugu, Nigeria., Anyaehie UE; Department of Orthopaedics and Trauma, National Orthopaedic Hospital, Enugu, Nigeria., Obadaseraye OR; Department of Surgery, Asaba Specialist Hospital, Asaba, Nigeria., Ogbonnaya IS; Department of Plastic and Reconstructive Surgery, National Orthopaedic Hospital, Enugu, Nigeria., Ogbu DC; Department of Orthopaedics and Trauma, National Orthopaedic Hospital, Enugu, Nigeria., Ngwangwa CL; Department of Orthopaedics and Trauma, National Orthopaedic Hospital, Enugu, Nigeria.

Publikováno v: Nigerian journal of clinical practice [Niger J Clin Pract] 2023 Jul; Vol. 26 (7), pp. 1029-1035.