Journal of Genetic Medicine : eISSN 2383-8442 / pISSN 1226-1769

Fig. 1.

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Fig. 1. Pedigree. The patient and his mother have the same genetic mutation. The patient was NF1 and LND affected simultaneously. His mother was NF1 affected and LND carrier as LND is an X-linked recessive disorder. NF1, neurofibromatosis type 1; LND, Lesch-Nyhan disease.
Journal of Genetic Medicine 2022;19:94-9
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