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beta-N-acetylhexosaminidase A in measurement

Indications: - evaluation of Tay-Sachs disease Clinical significance: - defects in HEXA are the cause of Tay-Sachs disease

Related

beta N-acetyl hexosaminidase alpha chain (hexosaminidase-A, HEXA) HEXA gene mutation; beta-N-acetylhexosaminidase alpha gene mutation

Specific

beta-N-acetylhexosaminidase A in amniotic fluid beta-N-acetylhexosaminidase A in dried blood spot beta-N-acetylhexosaminidase A in fibroblasts beta-N-acetylhexosaminidase A in leukocytes beta-N-acetylhexosaminidase A in serum

General

beta-N-acetylhexosaminidase measurement

References

Snomed