Table 1.
Patient | Age at onset, sex | Current age | STAT3 variant* | Autoimmunity | Lymphoproliferation | Postnatal short stature† | ||||
---|---|---|---|---|---|---|---|---|---|---|
Hematologic | Endocrine | GI | Other | LAD | Other | |||||
1 | 4y, M | 10y | p.G421R | AIHA | No | Hepatitis | Scleroderma, polyarthritis | Yes | HSM | Yes |
2 | 7y, M | 31y | p.T663I | AIHA, AITP | No | No | No | Yes | HSM | No |
3 | 3y, M | 25y | p.R152W | AIHA, AITP | IDDM | No | Alopecia, lung nodules | Yes | HSM | No |
4 | 13y, M | 32y | p.V353F | AIHA, AITP, AIN | No | No | Inflammatory lung disease | Yes | No | No |
5 | 3y, F | 5y | p.Q344H | AIHA | No | Enteropathy | LIP | Yes | HSM | Yes |
6 | 5y, F | 9y | p.E415K | none | IDDM | Enteropathy, achalasia | Atopic dermatitis | Yes | HSM | Yes |
7 | <1y, F | 23y | p.T716M | AIHA, AITP, AIN | Hypothyroid | Enteropathy | No | No | No | Yes |
8 | 3y, F | Dec 11y | p.N420K | AIHA, AITP, AIN | No | No | Polyarthritis | Yes | No | No |
Family 1 | ||||||||||
9, Proband | <1y, F | 26y | p.A703T | AIHA, AITP, AIN | No | Small bowel thickening | LIP, atopic dermatitis, alopecia | Yes | HSM | Yes |
10, Father | 15y, M | Dec 28y | p.A703T | AIHA, AIN | No | No | LIP | Yes | HSM | n/a |
11, Sibling | 12y, F | 24y | p.A703T | AITP, AIN | No | No | No | Yes | HSM | n/a |
Family 2 | ||||||||||
12, Proband | <1y, M | 4y | p.T716M | none | No | Enteropathy | No | No | No | Yes |
13, Father | EO, M | 32y | p.T716M | AITP | No | Enteropathy | No | No | Hodgkin lymphoma | Yes‡ |
LAD, lymphadenopathy; EO, early childhood onset; Dec, deceased; AIHA, autoimmune hemolytic anemia; AITP, autoimmune thrombocytopenia; AIN, autoimmune neutropenia; IDDM, insulin-dependent diabetes mellitus; LIP, lymphocytic interstitial pneumonia; HSM, hepatosplenomegaly; n/a, not available.
Amino acid substitution based on coding sequence of NM_139276.2.
Less than fifth percentile.
Percentile n/a.