Skip to main content
. 2017 Oct 10;1(22):1959–1976. doi: 10.1182/bloodadvances.2017008078

Table 1.

Description of the 12 DBA-affected patients who have been analyzed in this study

DBA patients Sex Age* (mo) Hb* g/dL Reticulocyte count,* ×109/L eADA activity Mutated gene Malformations Treatment*
UPN#987 F 2 4.2 2 NA RPS19 Yes T
Thumb anomaly
UPN#251 F 6 NA NA NA RPS19 No TI
UPN#35 F 3 5.6 NA Increased RPS19 Yes T
Hair anomaly
Prognathism
UPN#37 M 3 2.9 90 Normal RPS19 No T
UPN#412 M 2 7 NA Increased RPL5 Supernumerary thumb TI
Hypoplasic thumb
Flat thenar
UPN#587 M Birth 9.5 15 Increased RPL11 Yes S
Spina bifida
Triphalangeal thumb
Arnold Chiari
UPN#172 F Birth 4.5 23 Increased RPL11 No T
UPN#189 F 4 11.9 23 Increased RPL11 Yes S
Thumb anomaly
UPN#1130 M NA NA NA Increased RPL11 Yes TI
Thumb anomaly
Ear anomaly
Surdity
Ectopia testis
UPN#479 M Birth 6 NA Increased RPL11 Yes T
Prematurity
Triphalangeal thumb
Hypospadias
Heart malformation
UPN#1099 M 1 6.4 9 Increased RPL11 Yes T
Hypoacousia
Eye anomaly
Multiple naevi
UPN#412 M 2 7 NA Increased RPL11 Supernumerary thumb TI
Hypoplasic thumb
Flat thenar

eADA, erythrocyte adenosine deaminase; F, female; Hb, hemoglobin; M, male; NA, not available; S, steroid; T, transfusion dependence; TI, therapeutic independence.

*

At diagnosis.