Peroxisomal disorders are a group of hereditary metabolic disorders that occur when peroxisomes are missing or do not function correctly in the body. These disorders detected early or detected can help in the course of management and treatment. These tests include Enzyme assay can detect many disorders such as
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chevron_rightZellweger spectrum
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chevron_rightX-Linked adrenoleukodystrophy (ALD)
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chevron_rightRefsum disease
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chevron_rightRhizomelic chondrodysplasia punctata (RCDP)
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chevron_rightKrabbe’s disease
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chevron_rightGaucher's disease
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chevron_rightNiemann pick disease
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chevron_rightFabry’s disease
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chevron_rightMucopolysaccharidosis (MPS)
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chevron_rightMPS 1 H – Hurler Syndrome
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stopMPS1H/S- Hurler-Scheie syndrome
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stopMPS2- Hunter Syndrome
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stopMPS3A- Sanfilippo syndrome A
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stopMPS3B- Sanfilippo syndrome B
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stopMPS3C- Sanfilippo syndrome C
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stopMPS3D- Sanfilippo syndrome D
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stopMPS4A- Morquio syndrome B
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stopMPS4A- Morquio syndrome B
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stopMPS6- Maroteaux-Lamy syndrome
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stopMPS7- Sly syndrome