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. 2010 Jun 30;63(7):626–629. doi: 10.1136/jcp.2010.077560

Table 2.

Carrier rates by ethnic category* and Hb type: April 2005 to March 2007

Results for newborns: April 2005 to March 2007 FAS FAC FAD FAE Other Carriers
No. Rate per 1000 babies screened No. Rate per 1000 babies screened No. Rate per 1000 babies screened No. Rate per 1000 babies screened No. Rate per 1000 babies screened No. of babies screened
White British 376 0.55 121 0.18 249 0.37 77 0.11 435 0.64 679911
Bangladeshi 10 0.68 8 0.54 42 2.86 610 41.54 34 2.32 14686
Pakistani 28 0.87 5 0.15 264 8.18 61 1.89 75 2.32 32289
Chinese 7 1.44 1 0.21 0 0.00 22 4.52 14 2.88 4863
Any other White background 79 1.95 19 0.47 20 0.49 13 0.32 36 0.89 40469
White Irish 4 2.02 0 0.00 0 0.00 1 0.51 1 0.51 1978
White and Asian 25 2.68 2 0.21 21 2.25 149 15.98 17 1.82 9324
Any other Asian background 40 3.39 3 0.25 42 3.56 77 6.52 24 2.03 11806
Indian 115 4.62 9 0.36 176 7.07 43 1.73 57 2.29 24900
Not stated 1290 9.58 287 2.13 137 1.02 145 1.08 186 1.38 134693
Any other ethnic category 432 17.18 77 3.06 34 1.35 90 3.58 54 2.15 25145
Any other mixed background 339 21.00 99 6.13 17 1.05 70 4.34 23 1.42 16141
White and Black Caribbean 515 49.15 157 14.98 5 0.48 27 2.58 15 1.43 10479
White and Black African 422 75.51 68 12.17 1 0.18 1 0.18 11 1.97 5589
Any other Black background 273 81.66 64 19.14 4 1.20 1 0.30 11 3.29 3343
Black Caribbean 1093 86.80 383 30.42 2 0.16 0 0.00 26 2.06 12592
Black African 4952 120.88 863 21.07 8 0.20 4 0.10 102 2.49 40965
Total 10000 9.35 2166 2.03 1022 0.96 1391 1.30 1121 1.05 1069173

Birmingham was unable to provide denominators by ethnic category due to variations in coding of ethnic category and laboratory software constraints and their data has been taken out of this table. About 11% of all babies, 10% of carriers and approx 6% of all affected babies are tested in Birmingham.

Note that Portsmouth provided data from April 2006 and Oxford from July 2006 only.

*

Ethnic category as it appears on the Guthrie card.

Since there are many ‘D’ variants and characterisation may take some time, it is recommended that all ‘D’ variants with the characteristics of D Punjab (the only clinically significant variant) are assumed to be clinically significant and reported. DNA analysis or mass spectrometry can be used to elucidate the diagnosis.