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Published in 2021 at "World Journal of Clinical Cases"
DOI: 10.12998/wjcc.v9.i29.8839
Abstract: BACKGROUND Neurofibromatosis type 1 (NF1) is an inherited autosomal dominant disorder affecting many parts of the body with cafĂ© au lait spots, skeletal deformity, and scoliosis. A familial case of NF1 with scoliosis and a…
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Keywords:
familial left;
case;
neurofibromatosis;
left cervical ... See more keywords