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. 2006 Sep 18;7:72. doi: 10.1186/1471-2350-7-72

Table 5.

Clinical data of patients with TSC1 mutations

Family no. Familial/Sporadic Mutation type Sex Onset age of seizure Intellectual performance Brain tubers Renal tumors Hepatic tumors Cardiac rhabdomyoma Hypomelanotic macules Facial angiofibroma Shagreen patch Ungual fibroma
2 F FS F 2 y N + 0 NA NA 0 + 0 +
3 S NM M 8 y 3 m N + 0 0 0 + + + 0
41 S NM F 1 y N + 0 0 + + 0 0 0
31 S NM F 6 m LD + + 0 + + 0 0 0
36 S FS M 2 y N + 0 0 0 + + 0 0
61 F NM M 3 y 6 m LD + 0 0 0 + + 0 0
62 S FS M 1 m LD + + 0 0 + + + +
72 S FS M 3 y N + 0 0 + + 0 + 0

N: normal or no seizure, LD: learning disorder, MR: metal retardation, NA: not available.