Table 7.
Region 7 newborn screening incidence data for selected metabolic conditions from January 1, 2001 – December 31, 2010
Newborn Screening Programs in Region 7 | ||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|
Condition | Alaskaa | Californiab | Hawaiic | Idahod | Oregone | Washingtonf | ||||||
Cases | Births | Cases | Births | Cases | Births | Cases | Births | Cases | Births | Cases | Births | |
3-MCC | 1 | 86,374 | 58 | 2,997,046 | 3 | 149,783 | 1 | 184,644 | 8 | 428,110 | 0 | 220,866 |
ASA | 0 | 86,374 | 7 | 2,997,046 | 1 | 149,783 | 1 | 184,644 | 5 | 428,110 | 0 | 220,866 |
BIO | 1 | 106,126 | 25 | 1,875,211 | 1 | 184,422 | 1 | 244,254 | 4 | 474,310 | 4 | 605,494 |
Partial BIO | 3 | 106,126 | 33 | 1,875,211 | 5 | 184,422 | 8 | 244,254 | 15 | 474,310 | 16 | 605,494 |
BKT | 0 | 86,374 | 2 | 2,997,046 | 0 | 149,783 | 0 | 184,644 | 0 | 288,758 | 1 | 220,866 |
CBL A,B | 0 | 44,851 | 6 | 2,997,046 | 0 | 149,783 | 0 | 184,644 | 0 | 428,110 | 0 | 220,866 |
CUD | 0 | 86,374 | 41 | 2,997,046 | 0 | 149,783 | 2 | 184,644 | 2 | 428,110 | 0 | 220,866 |
CIT | 0 | 86,374 | 10 | 2,997,046 | 0 | 149,783 | 2 | 184,644 | 1 | 428,110 | 0 | 220,866 |
GA-1 | 3 | 86,374 | 24 | 2,997,046 | 1 | 149,783 | 3 | 184,644 | 2 | 428,110 | 3 | 220,866 |
GALT | 11 | 106,126 | 59 | 5,417,932 | 2 | 184,422 | 4 | 225,254 | 5 | 474,310 | 7 | 843,161 |
HCY | 0 | 86,374 | 2 | 2,997,046 | 0 | 167,295 | 0 | 205,093 | 1 | 382,057 | 1 | 605,494 |
HMG | 0 | 86,374 | 1 | 2,997,046 | 0 | 149,783 | 0 | 184,644 | 0 | 428,110 | 0 | 220,866 |
IVA | 0 | 86,374 | 21 | 2,997,046 | 2 | 149,783 | 1 | 184,644 | 1 | 428,110 | 0 | 220,866 |
LCHADD | 0 | 86,374 | 6 | 2,997,046 | 0 | 149,783 | 1 | 184,644 | 4 | 428,110 | 0 | 220,866 |
MCADD | 9 | 86,374 | 115 | 2,997,046 | 4 | 149,783 | 16 | 184,644 | 28 | 428,110 | 32 | 605,494 |
MCD | 0 | 86,374 | 3 | 2,997,046 | 1 | 149,783 | 0 | 184,644 | 0 | 288,758 | 0 | 220,866 |
MSUD | 2 | 106,126 | 21 | 2,997,046 | 2 | 184,422 | 2 | 225,254 | 0 | 474,310 | 2 | 605,494 |
MUT | 0 | 86,374 | 44 | 2,997,046 | 0 | 149,783 | 3 | 184,644 | 5 | 428,110 | 1 | 427,302 |
PKU | 7 | 106,126 | 171 | 5,417,932 | 1 | 184,422 | 15 | 225,254 | 20 | 474,310 | 52 | 843,161 |
PKU Variant | 0 | 106,126 | 139 | 5,417,932 | 1 | 184,422 | 1 | 225,254 | 6 | 474,310 | 31 | 843,161 |
PROP | 2 | 86,374 | 6 | 2,997,046 | 0 | 149,783 | 1 | 184,644 | 0 | 428,110 | 0 | 220,866 |
TFP | 0 | 86,374 | 2 | 2,997,046 | 0 | 149,783 | 0 | 184,644 | 0 | 288,758 | 0 | 220,866 |
TYR-I | 1 | 86,374 | 10 | 2,997,046 | 0 | 149,783 | 0 | 184,644 | 0 | 428,110 | 0 | 220,866 |
VLCADD | 3 | 86,374 | 37 | 2,997,046 | 7 | 149,783 | 3 | 184,644 | 3 | 428,110 | 5 | 220,866 |
Data began: Jan 1, 2003 for all except BIO, CBL A,B, GALT, MSUD, PKU; Jan 1, 2007 for CBL A,B
Data began: Jul 11, 2005 for all except BIO, GALT, PKU; Jul 16, 2007 for BIO
Data began: Jan 1, 2002 for HCY; Jan 1, 2003 for all except BIO, GALT, HCY, MSUD, PKU
Data began: Jan 1, 2002 for HCY; Jan 1, 2003 for all except BIO, GALT, HCY, MSUD, PKU
Data began: Jan 1, 2002 for all except BIO, BKT, GALT, HCY, MCD, MSUD, PKU, TFP; Jan 1, 2003 for HCY; Jan 1, 2005 for BKT, MCD, TFP
Data began: Jan 1, 2004 for BIO, HCY, MCADD, MSUD; Jul 1, 2008 for all except BIO, GALT, HCY, MCADD, MSUD, PKU
Abbreviations: 3-MCC, 3-Methylcrotonyl-CoA carboxylase deficiency; ASA, Argininosuccinic aciduria; BIO, biotinidase; BKT, Beta-ketothiolase deficiency; CBL A,B, methylmalonic acidemia (cobalamin A and B); CIT, Citrullinemia; CUD, Carnitine uptake defect; GA-1, Glutaric acidemia type I; GALT, Galactosemia transferase deficiency (classical galactosemia); HCY, Homocystinuria; HMG, 3-Hydroxy 3-methyl glutaric aciduria; IVA, Isovaleric acidemia; LCHADD, Long-chain L-3- hydroxyacyl-CoA dehydrogenase deficiency; MCADD, Medium-chain acyl-CoA dehydrogenase deficiency; MCD, Multiple carboxylase deficiency; MSUD, Maple syrup (urine) disease; MUT, Methylmalonic academia (methylmalonyl-CoA mutase deficiency); PKU, Phenylketonuria; PROP, Propionic acidemia; TFP, Trifunctional protein deficiency; TYR-I, Tyrosinemia type I; VLCADD, Very long-chain acyl-CoA dehydrogenase deficiency