Table 1.
Patient | Country of origin | Gender | Age at diagnosis and presenting features | EIF2AK3 mutation | Acute hepatitis – age at 1st episode and frequency | Acute hepatic failure –age at onset, number, and outcomes | Other features | Prognosis/comments |
1.1 | KSA | Male | Hyperglycaemia at 8 weeks | p.W430X (c.1290G>A) | 1 episode at 8 months | No | No | Alive at 18 months old |
2.1 [17] | KSA | Male | DKA at 21 weeks | p.V349Sfs*3 (c.l044_1057del) | 20 months; 8 episodes (first after reporting) | 1 fatal episode at 6 years | SD, SS, FTT and impaired RF during hepatitis | Died at 6 years |
3.1 [4, 17] | KSA | Female | DKA and hepatitis at 8 weeks | p.V349Sfs*3 (c.l044_1057del) | 8 weeks; 20 episodes | 2 episodes at 3 years and 1 fatal at 7.5 years | No | Died at 7.5 years (after initial reporting) |
3.2 [17] | KSA | Female | DKA and hepatitis at 10 weeks | p.V349Sfs*3 (c.l044_1057del) | 10 weeks; 8 episodes | 1 fatal episode at 2 years | SD, SS and impaired RF during hepatitis | Died at 2 years |
3.3 [17] | KSA | Male | Hyperglycaemia at 6 weeks | p.V349Sfs*3 (c.l044_1057del) | 2 years; once proceeded to acute hepatic failure | 1 fatal episode at 2 years | No | Died at 2 years |
4.1 [17] | KSA | Male | DKA at 8 weeks | p.V349Sfs*3 (c.l044_1057del) | 18 months; 4 episodes (first after reporting) | 1 episode (after first reporting) | No | Alive at 6 years |
5.1a | KSA | Male | Hyperglycaemia at 2 years | P.W163X (c.491G>A) | 2.4 years; once proceeded to acute hepatic failure | 1 treated conservatively | Impaired RF during hepatitis episode | Alive at 5 years |
6.1a | KSA | Male | Hyperglycaemia at 1.5 years | p.N420Tfs*14 (c.l259del) | 2.5 years; once proceeded to hepatic failure | 1 fatal episode at 7 years | SD, SS and impaired RF during hepatitis | Died at 7 years |
7.1 | Jordan | Male | DKA and hepatitis at 6 weeks | p.G1010D (c.3029G>A) | 6 weeks; 4 episodes | 1 fatal episode at 3.5 years | SD, SS, PH, ASD, DD and epilepsy | Died at 3.5 years |
8.1a | Kuwait | Male | Hyperglycaemia at 15 days | FS 523STOP (delGAAA1639-42) | 10 months; once proceeded to acute hepatic failure | 1 fatal episode at 10.5 months | Impaired RF during hepatitis episode | Died at 10.5 months |
9.1 | Iraq | Male | Hyperglycaemia at 7 weeks | p.W520X (c.1560G>A) | No | No | No | Alive at 14 months; siblings died of WRS |
10.1 | Lebanon | Female | DKA at 11 weeks | p.R1064X (c.3190C>T) | 11 months; 1 episode recovered spontaneously | No | Impaired RF during hepatitis and deafness | Alive at 15 months; siblings died of WRS |
11.1 | Oman | Male | Hyperglycaemia at 4 weeks | P.Y588X (c.1764T>G) | 10 months; 6 episodes | 2 episodes, 1 led to death | Neutropenia, SD, SS, FTT, DD and ADHD | Died at 6.5 years; had liver biopsy for persistent hepatomegaly |
11.2 | Oman | Female | DKA and hepatitis at 6 weeks | P.Y588X (c.1764T>G) | 6 weeks; 5 episodes | 1 treated conservatively | Neutropenia and FTT | Alive at 5 years |
12.1 | UAE | Female | DKA at 6 weeks | p.W430X (c.!290G>A) | 8 weeks; 9 episodes | 1 treated conservatively | Anaemia and RH | Alive at 10 months; had liver biopsy |
12.2 | UAE | Female | DKA at 10 weeks | p.W430X (c.1290G>A) | 11 weeks; 7 episodes | 4 episodes treated conservatively | SD, SS anaemia, neutropenia, squint and RH | Alive at 2.5 years; had liver biopsy |
12.3 [4] | UAE | Male | DKA and hepatitis at 7 weeks | p.W430X (c.1290G>A) | 7 weeks; 7 further episodes | 1 fatal episode | SD, SS, anaemia, neutropenia and RH | Died at 7 years |
12.4 [4] | UAE | Male | DKA and hepatitis at 6 weeks | p.W430X (c.1290G>A) | 6 weeks; >8 episodes | 3 episodes, 1 resulted in death | SD, SS, anaemia, neutropenia and RH | Died at 4 years |
12.5 [4] | UAE | Male | DKA at 6 weeks | p.W430X (c.1290G>A) | 8 weeks; once/3 months | 6 episodes, 1 resulted in death | SD, SS, anaemia, neutropenia and RH | Died at 5 years |
12.6 | UAE | Female | Hyperglycaemia and hepatitis at 7 weeks | p.W430X (c.1290G>A) | 7 weeks; 6 episodes | 4 episodes treated conservatively | Pancytopenia, FTT and RH | Alive at 2.4 years; had liver biopsy |
13.1 [4] | UAE | Male | Hyperglycaemia at 14 months | P.I650T (c.1949T>C) | 1 episode at 2 years; none since transplant | 1 episode led to transplant | Anaemia, SD and SS | Alive at 8 years |
14.1 [4] | UAE | Male | DKA at 8 weeks | P.G956E (c.2867G>A) | 10 weeks; >15 episodes | 1 fatal episode (after reporting) | SD, SS and anaemia | Died at 15 years (after initial reporting) |
15.1 | UAE | Male | Hyperglycaemia at 8 weeks | P.E524X (c.l567_1570del) | 9 months; 3 episodes | 1 episode treated conservatively | SD and anaemia | Alive at 18 months |
16.1 | UAE | Female | DKA at 6 weeks | p.? (c.1427-?_2490+?del) | 8 months; 2 episodes | 1 fatal episode | No | Died at 2.9 years |
17.1 | Kuwait | Male | Hyperglycaemia at 2 months | P.S991N (c.2972G>A) | 14 months; 2 episodes | 2 episodes treated conservatively | DD, SD, SS and PH | Alive at 17.5 years |
18.1 | Sudan | Male | Hyperglycaemia, at 2 months | p.P269fs (c.802_803dup) | No | No | DD and SD | Alive at 3.5 years |
19.1 | Sudan | Female | Hyperglycaemia at 2 months | P.Y989X (c.2967T>A) | No | No | No | Alive at 3 years; twin brother healthy |
20.1 | Sudan | Male | Hyperglycaemia at 2 months | p.? (c.1647+2T>A) | No | No | FTT | Alive at 2 years |
All mutations listed are homozygous. KSA = Kingdom of Saudi Arabia; UAE = United Arab Emirates; DKA = diabetic ketoacidosis; FTT = failure to thrive; SS = short stature; RF = renal function; ADHD = attention deficit hyperactivity disorder; ASD = atrial septal defect; RH = recurrent hypoglycaemia; DD = developmental delay. All nucleotide and amino acid numbering refers to transcript AF110146.1, which contains 7 leucine residues in the microsatellite region of exon one. The c.l427-?_2490+?del and c.1647+2T>A mutations have been listed at the protein level as p.?, which denotes that the protein has not been analyzed, although an effect is expected.
These samples were tested outside Exeter.