New Testing Breakthroughs in AACC's Clinical Chemistry Journal Could Give Hope to Families of Children With Two Rare Genetic Diseases

For the first time, researchers have developed tests that could improve the diagnosis of two rare childhood diseases known as congenital disorders of glycosylation (CDGs) and metachromatic leukodystrophy, and that could even lead to new treatments for CDGs. The findings were published in the Mass Spectrometry issue of Clinical Chemistry, the journal of AACC.

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