TOPICS: Ornithine transcarbamylase deficiency, X-linked adrenoleukodystrophy, Duchenne muscular dystrophy, Becker muscular dystrophy, Hunter syndrome, ocular albinism, Bruton agammaglobulinemia, Wiskott-Aldrich syndrome, Lesch-Nyhan syndrome, Hyper-IgM syndrome, hemophilia A, hemophilia B, severe combined immunodeficiency (SCID), Menkes disease, G6PD deficiency, Fabry disease
