A scarce case: Co-occurrence of neurofibromatosis type 1 and Klinefelter syndrome
{{output}}
Neurofibromatosis type 1 (NF1) is an autosomal dominant disorder with a heterogeneous group of symptoms, including characteristic cafe-au-lait macules, axillary or inguinal freckling, Lisch nodules, as well as skeletal deformation, scoliosis, mental retardatio... ...
